Label: MYCOPHENOLATE MOFETIL- mycophenolate mofetil capsule MYCOPHENOLATE MOFETIL- mycophenolate mofetil tablet, film coated 

  • NDC Code(s): 0093-7334-01, 0093-7334-05, 0093-7477-01, 0093-7477-05
  • Packager: Teva Pharmaceuticals USA Inc
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated 05/14

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  • BOXED WARNING(What is this?)

    WARNING: EMBRYOFETAL TOXICITY, MALIGNANCIES AND SERIOUS INFECTIONS

    Use during pregnancy is associated with increased risks of first trimester pregnancy loss and congenital malformations. Females of reproductive potential (FRP) must be counseled regarding pregnancy prevention and planning (see WARNINGS and PRECAUTIONS).

    Immunosuppression may lead to increased susceptibility to infection and possible development of lymphoma. Only physicians experienced in immunosuppressive therapy and management of renal, cardiac or hepatic transplant patients should prescribe mycophenolate mofetil. Patients receiving the drug should be managed in facilities equipped and staffed with adequate laboratory and supportive medical resources. The physician responsible for maintenance therapy should have complete information requisite for the follow-up of the patient (see WARNINGS and PRECAUTIONS).

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  • DESCRIPTION

    Mycophenolate mofetil, USP is the 2-morpholinoethyl ester of mycophenolic acid (MPA), an immunosuppressive agent; inosine monophosphate dehydrogenase (IMPDH) inhibitor.

    The chemical name for mycophenolate mofetil, USP (MMF) is 2-morpholinoethyl (E)-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoate. It has the following structural formula:

    structural formula for mycophenolate mofetil

    C23H31NO7 M.W. 433.50

    Mycophenolate mofetil, USP is a white to almost white crystalline powder. It is slightly soluble in water (43 mcg/mL at pH 7.4), freely soluble in acetone, soluble in methanol, sparingly soluble in anhydrous ethanol, and practically insoluble in water. No polymorphic form was found. The apparent partition coefficient in 1-octanol/water (pH 7.4) buffer solution is 238. The pKa values for mycophenolate mofetil, USP are 5.6 for the morpholino group and 8.5 for the phenolic group.

    Mycophenolate mofetil, USP is available for oral administration as capsules containing 250 mg of mycophenolate mofetil, USP and as tablets containing 500 mg of mycophenolate mofetil, USP.

    Inactive ingredients in mycophenolate mofetil capsules USP, 250 mg include: black iron oxide, croscarmellose sodium, D&C red #28, D&C yellow #10, FD&C blue #1, FD&C red #40, gelatin, magnesium stearate, povidone, pregelatinized starch, propylene glycol, shellac glaze, and titanium dioxide.

    Inactive ingredients in mycophenolate mofetil tablets USP, 500 mg include: croscarmellose sodium, FD&C blue #2 aluminum lake, FD&C red #40 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, talc, and titanium dioxide.

    Mycophenolate mofetil tablets USP meet USP Dissolution Test 3.

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  • CLINICAL PHARMACOLOGY

    Mechanism of Action

    Mycophenolate mofetil has been demonstrated in experimental animal models to prolong the survival of allogeneic transplants (kidney, heart, liver, intestine, limb, small bowel, pancreatic islets, and bone marrow).

    Mycophenolate mofetil has also been shown to reverse ongoing acute rejection in the canine renal and rat cardiac allograft models. Mycophenolate mofetil also inhibited proliferative arteriopathy in experimental models of aortic and cardiac allografts in rats, as well as in primate cardiac xenografts. Mycophenolate mofetil was used alone or in combination with other immunosuppressive agents in these studies. Mycophenolate mofetil has been demonstrated to inhibit immunologically mediated inflammatory responses in animal models and to inhibit tumor development and prolong survival in murine tumor transplant models.

    Mycophenolate mofetil is rapidly absorbed following oral administration and hydrolyzed to form MPA, which is the active metabolite. MPA is a potent, selective, uncompetitive, and reversible inhibitor of inosine monophosphate dehydrogenase (IMPDH), and therefore inhibits the de novo pathway of guanosine nucleotide synthesis without incorporation into DNA. Because T- and B-lymphocytes are critically dependent for their proliferation on de novo synthesis of purines, whereas other cell types can utilize salvage pathways, MPA has potent cytostatic effects on lymphocytes. MPA inhibits proliferative responses of T- and B-lymphocytes to both mitogenic and allospecific stimulation. Addition of guanosine or deoxyguanosine reverses the cytostatic effects of MPA on lymphocytes. MPA also suppresses antibody formation by B-lymphocytes. MPA prevents the glycosylation of lymphocyte and monocyte glycoproteins that are involved in intercellular adhesion to endothelial cells and may inhibit recruitment of leukocytes into sites of inflammation and graft rejection. Mycophenolate mofetil did not inhibit early events in the activation of human peripheral blood mononuclear cells, such as the production of interleukin-1 (IL-1) and interleukin-2 (IL-2), but did block the coupling of these events to DNA synthesis and proliferation.

    Pharmacokinetics

    Following oral and intravenous administration, mycophenolate mofetil undergoes rapid and complete metabolism to MPA, the active metabolite. Oral absorption of the drug is rapid and essentially complete. MPA is metabolized to form the phenolic glucuronide of MPA (MPAG) which is not pharmacologically active. The parent drug, mycophenolate mofetil, can be measured systemically during the intravenous infusion; however, shortly (about 5 minutes) after the infusion is stopped or after oral administration, MMF concentration is below the limit of quantitation (0.4 mcg/mL).

    Absorption

    In 12 healthy volunteers, the mean absolute bioavailability of oral mycophenolate mofetil relative to intravenous mycophenolate mofetil (based on MPA AUC) was 94%. The area under the plasma-concentration time curve (AUC) for MPA appears to increase in a dose­proportional fashion in renal transplant patients receiving multiple doses of mycophenolate mofetil up to a daily dose of 3 g (see Table 1).

    Food (27 g fat, 650 calories) had no effect on the extent of absorption (MPA AUC) of mycophenolate mofetil when administered at doses of 1.5 g bid to renal transplant patients. However, MPA Cmax was decreased by 40% in the presence of food (see DOSAGE AND ADMINISTRATION).

    Distribution

    The mean (± SD) apparent volume of distribution of MPA in 12 healthy volunteers is approximately 3.6 (± 1.5) and 4 (± 1.2) L/kg following intravenous and oral administration, respectively. MPA, at clinically relevant concentrations, is 97% bound to plasma albumin. MPAG is 82% bound to plasma albumin at MPAG concentration ranges that are normally seen in stable renal transplant patients; however, at higher MPAG concentrations (observed in patients with renal impairment or delayed renal graft function), the binding of MPA may be reduced as a result of competition between MPAG and MPA for protein binding. Mean blood to plasma ratio of radioactivity concentrations was approximately 0.6 indicating that MPA and MPAG do not extensively distribute into the cellular fractions of blood.

    In vitro studies to evaluate the effect of other agents on the binding of MPA to human serum albumin (HSA) or plasma proteins showed that salicylate (at 25 mg/dL with HSA) and MPAG (at ≥ 460 mcg/mL with plasma proteins) increased the free fraction of MPA. At concentrations that exceeded what is encountered clinically, cyclosporine, digoxin, naproxen, prednisone, propranolol, tacrolimus, theophylline, tolbutamide, and warfarin did not increase the free fraction of MPA. MPA at concentrations as high as 100 mcg/mL had little effect on the binding of warfarin, digoxin or propranolol, but decreased the binding of theophylline from 53% to 45% and phenytoin from 90% to 87%.

    Metabolism

    Following oral and intravenous dosing, mycophenolate mofetil undergoes complete metabolism to MPA, the active metabolite. Metabolism to MPA occurs presystemically after oral dosing. MPA is metabolized principally by glucuronyl transferase to form the phenolic glucuronide of MPA (MPAG) which is not pharmacologically active. In vivo, MPAG is converted to MPA via enterohepatic recirculation. The following metabolites of the 2-hydroxyethyl-morpholino moiety are also recovered in the urine following oral administration of mycophenolate mofetil to healthy subjects: N-(2-carboxymethyl)-morpholine, N-(2-hydroxyethyl)-morpholine, and the N-oxide of N-(2-hydroxyethyl)-morpholine.

    Secondary peaks in the plasma MPA concentration-time profile are usually observed 6 to 12 hours postdose. The coadministration of cholestyramine (4 g tid) resulted in approximately a 40% decrease in the MPA AUC (largely as a consequence of lower concentrations in the terminal portion of the profile). These observations suggest that enterohepatic recirculation contributes to MPA plasma concentrations.

    Increased plasma concentrations of mycophenolate mofetil metabolites (MPA 50% increase and MPAG about a 3 fold to 6 fold increase) are observed in patients with renal insufficiency (see CLINICAL PHARMACOLOGY, Special Populations).

    Excretion

    Negligible amount of drug is excreted as MPA (< 1% of dose) in the urine. Orally administered radiolabeled mycophenolate mofetil resulted in complete recovery of the administered dose, with 93% of the administered dose recovered in the urine and 6% recovered in feces. Most (about 87%) of the administered dose is excreted in the urine as MPAG. At clinically encountered concentrations, MPA and MPAG are usually not removed by hemodialysis. However, at high MPAG plasma concentrations (> 100 mcg/mL), small amounts of MPAG are removed. Bile acid sequestrants, such as cholestyramine, reduce MPA AUC by interfering with enterohepatic circulation of the drug (see OVERDOSAGE).

    Mean (± SD) apparent half-life and plasma clearance of MPA are 17.9 (± 6.5) hours and 193 (± 48) mL/min following oral administration and 16.6 (± 5.8) hours and 177 (± 31) mL/min following intravenous administration, respectively.

    Pharmacokinetics in Healthy Volunteers, Renal, Cardiac, and Hepatic Transplant Patients

    Shown below are the mean (± SD) pharmacokinetic parameters for MPA following the administration of mycophenolate mofetil given as single doses to healthy volunteers and multiple doses to renal, cardiac, and hepatic transplant patients. In the early posttransplant period (< 40 days posttransplant), renal, cardiac, and hepatic transplant patients had mean MPA AUCs approximately 20% to 41% lower and mean Cmax approximately 32% to 44% lower compared to the late transplant period (3 to 6 months posttransplant).

    Mean MPA AUC values following administration of 1 g bid intravenous mycophenolate mofetil over 2 hours to renal transplant patients for 5 days were about 24% higher than those observed after oral administration of a similar dose in the immediate posttransplant phase. In hepatic transplant patients, administration of 1 g bid intravenous mycophenolate mofetil followed by 1.5 g bid oral mycophenolate mofetil resulted in mean MPA AUC values similar to those found in renal transplant patients administered 1 g mycophenolate mofetil bid.

    Table 1: Pharmacokinetic Parameters for MPA [Mean (± SD)] Following Administration of Mycophenolate Mofetil to Healthy Volunteers (Single Dose), Renal, Cardiac, and Hepatic Transplant Patients (Multiple Doses)
    *
    AUC (0 to 12h) values quoted are extrapolated from data from samples collected over 4 hours.
      Dose/Route Tmax (h)

    Cmax

    (mcg/mL)

    Total AUC

    (mcg•h/mL)

    Healthy Volunteers (single dose) 1 g/oral 0.80 (± 0.36) (n = 129) 24.5 (± 9.5) (n = 129) 63.9 (± 16.2) (n = 117)
    Renal Transplant Patients (bid dosing) Time After Transplantation Dose/Route   Tmax(h)

    Cmax

    (mcg/mL)

    Interdosing Interval AUC(0 to 12h)(mcg•h/mL)
    5 days 1 g/iv 1.58 (± 0.46) (n = 31) 12 (± 3.82) (n = 31) 40.8 (± 11.4) (n = 31)
    6 days 1 g/oral 1.33 (± 1.05) (n = 31) 10.7 (± 4.83) (n = 31) 32.9 (± 15) (n = 31)
    Early (< 40 days) 1 g/oral 1.31 (± 0.76) (n = 25) 8.16 (± 4.50) (n = 25) 27.3 (± 10.9) (n = 25)
    Early (< 40 days) 1.5 g/oral 1.21 (± 0.81) (n = 27) 13.5 (± 8.18) (n = 27) 38.4 (± 15.4) (n = 27)
    Late (> 3 months) 1.5 g/oral 0.90 (± 0.24) (n = 23) 24.1 (± 12.1) (n = 23) 65.3 (± 35.4) (n = 23)
    Cardiac Transplant Patients (bid dosing) Time After Transplantation Dose/Route   Tmax(h)

    Cmax

     (mcg/mL)

    Interdosing Interval AUC(0 to 12h)  

    (mcg•h/mL)

    Early (Day before discharge) 1.5 g/oral 1.8 (± 1.3) (n = 11) 11.5 (± 6.8) (n = 11) 43.3 (± 20.8) (n = 9)
    Late (> 6 months) 1.5 g/oral 1.1 (± 0.7) (n = 52) 20 (± 9.4) (n = 52) 54.1* (± 20.4) (n = 49)
    Hepatic Transplant Patients (bid dosing) Time After Transplantation Dose/Route Tmax(h)

    Cmax

    (mcg/mL)

    Interdosing Interval AUC(0 to 12h)  

    (mcg•h/mL)

    4 to 9 days 1 g/iv 1.50 (± 0.517) (n = 22) 17 (± 12.7) (n = 22) 34 (± 17.4) (n = 22)
    Early (5 to 8 days) 1.5 g/oral 1.15 (± 0.432) (n = 20) 13.1 (± 6.76) (n = 20) 29.2 (± 11.9) (n = 20)
    Late (> 6 months) 1.5 g/oral 1.54 (± 0.51) (n = 6) 19.3 (± 11.7) (n = 6) 49.3 (± 14.8) (n = 6)

    Two 500 mg tablets have been shown to be bioequivalent to four 250 mg capsules. Five mL of the 200 mg/mL constituted oral suspension have been shown to be bioequivalent to four 250 mg capsules.

    Special Populations

    Shown below are the mean (± SD) pharmacokinetic parameters for MPA following the administration of oral mycophenolate mofetil given as single doses to non-transplant subjects with renal or hepatic impairment.

    Table 2: Pharmacokinetic Parameters for MPA [Mean (± SD)] Following Single Doses of Mycophenolate Mofetil Capsules in Chronic Renal and Hepatic Impairment

    Renal Impairment

    (no. of patients)

    Dose Tmax (h)

    Cmax

    (mcg/mL)

    AUC(0 to 96h)

    (mcg•h/mL)

    Healthy Volunteers
    GFR > 80 mL/min/1.73 m2 (n
    = 6)
    1 g 0.75 (± 0.27) 25.3 (± 7.99) 45 (± 22.6)
    Mild Renal Impairment
    GFR 50 to 80 mL/min/1.73
    m2 (n = 6)
    1 g 0.75 (± 0.27) 26 (± 3.82) 59.9 (± 12.9)
    Moderate Renal Impairment
    GFR 25 to 49 mL/min/1.73
    m2 (n = 6)
    1 g 0.75 (± 0.27) 19 (± 13.2) 52.9 (± 25.5)
    Severe Renal Impairment
    GFR < 25 mL/min/1.73 m2 (n = 7)
    1 g 1 (± 0.41) 16.3 (± 10.8) 78.6 (± 46.4)

    Hepatic Impairment

    (no. of patients)

    Dose Tmax (h)

    Cmax

     (mcg/mL)

    AUC(0 to 48h)

    (mcg•h/mL)

    Healthy Volunteers
    (n = 6)
    1 g 0.63 (± 0.14) 24.3 (± 5.73) 29 (± 5.78)
    Alcoholic Cirrhosis
    (n = 18)
    1 g 0.85 (± 0.58) 22.4 (± 10.1) 29.8 (± 10.7)

    Renal Insufficiency

    In a single-dose study, MMF was administered as capsule or intravenous infusion over 40 minutes. Plasma MPA AUC observed after oral dosing to volunteers with severe chronic renal impairment [glomerular filtration rate (GFR) < 25 mL/min/1.73 m2] was about 75% higher relative to that observed in healthy volunteers (GFR > 80 mL/min/1.73 m2). In addition, the single-dose plasma MPAG AUC was 3 fold to 6 fold higher in volunteers with severe renal impairment than in volunteers with mild renal impairment or healthy volunteers, consistent with the known renal elimination of MPAG. No data are available on the safety of long-term exposure to this level of MPAG.

    Plasma MPA AUC observed after single-dose (1 g) intravenous dosing to volunteers (n = 4) with severe chronic renal impairment (GFR < 25 mL/min/1.73 m2) was 62.4 mcg•h/mL (± 19.3). Multiple dosing of mycophenolate mofetil in patients with severe chronic renal impairment has not been studied (see PRECAUTIONS,Patients With Renal Impairmentand DOSAGE AND ADMINISTRATION).

    In patients with delayed renal graft function posttransplant, mean MPA AUC(0 to 12h) was comparable to that seen in posttransplant patients without delayed renal graft function. There is a potential for a transient increase in the free fraction and concentration of plasma MPA in patients with delayed renal graft function. However, dose adjustment does not appear to be necessary in patients with delayed renal graft function. Mean plasma MPAG AUC(0 to 12h) was 2 fold to 3 fold higher than in posttransplant patients without delayed renal graft function (see PRECAUTIONS,Patients With Renal Impairmentand DOSAGE AND ADMINISTRATION).

    In 8 patients with primary graft non-function following renal transplantation, plasma concentrations of MPAG accumulated about 6 fold to 8 fold after multiple dosing for 28 days. Accumulation of MPA was about 1 fold to 2 fold.

    The pharmacokinetics of mycophenolate mofetil are not altered by hemodialysis. Hemodialysis usually does not remove MPA or MPAG. At high concentrations of MPAG (> 100 mcg/mL), hemodialysis removes only small amounts of MPAG.

    Hepatic Insufficiency

    In a single-dose (1 g oral) study of 18 volunteers with alcoholic cirrhosis and 6 healthy volunteers, hepatic MPA glucuronidation processes appeared to be relatively unaffected by hepatic parenchymal disease when pharmacokinetic parameters of healthy volunteers and alcoholic cirrhosis patients within this study were compared. However, it should be noted that for unexplained reasons, the healthy volunteers in this study had about a 50% lower AUC as compared to healthy volunteers in other studies, thus making comparisons between volunteers with alcoholic cirrhosis and healthy volunteers difficult. Effects of hepatic disease on this process probably depend on the particular disease. Hepatic disease with other etiologies, such as primary biliary cirrhosis, may show a different effect. In a single-dose (1 g intravenous) study of 6 volunteers with severe hepatic impairment (aminopyrine breath test less than 0.2% of dose) due to alcoholic cirrhosis, MMF was rapidly converted to MPA. MPA AUC was 44.1 mcg•h/mL (± 15.5).

    Pediatrics

    The pharmacokinetic parameters of MPA and MPAG have been evaluated in 55 pediatric patients (ranging from 1 year to 18 years of age) receiving mycophenolate mofetil oral suspension at a dose of 600 mg/m2 bid (up to a maximum of 1 g bid) after allogeneic renal transplantation. The pharmacokinetic data for MPA is provided in Table 3:

    Table 3: Mean (± SD) Computed Pharmacokinetic Parameters for MPA by Age and Time After Allogeneic Renal Transplantation
    *
    adjusted to a dose of 600 mg/m 2
    a subset of 1 to < 6 yr
    n = 20
    §
    n = 16
    Age Group (n) Time Tmax (h) Dose Adjusted* Cmax (mcg/mL) Dose Adjusted* AUC0 to 12 (mcg•h/mL)
    1 to < 2 yr (6) Early (Day 7) 3.03 (4.70) 10.3 (5.80) 22.5 (6.66)
    1 to < 6 yr (17) 1.63 (2.85) 13.2 (7.16) 27.4 (9.54)
    6 to < 12 yr (16) 0.940 (0.546) 13.1 (6.30) 33.2 (12.1)
    12 to 18 yr (21) 1.16 (0.830) 11.7 (10.7) 26.3 (9.14)
    1 to < 2 yr (4) Late (Month 3) 0.725 (0.276) 23.8 (13.4) 47.4 (14.7)
    1 to < 6 yr (15) 0.989 (0.511) 22.7 (10.1) 49.7 (18.2)
    6 to < 12 yr (14) 1.21 (0.532) 27.8 (14.3) 61.9 (19.6)
    12 to 18 yr (17) 0.978 (0.484) 17.9 (9.57) 53.6 (20.3)§
    1 to < 2 yr (4) Late (Month 9) 0.604 (0.208) 25.6 (4.25) 55.8 (11.6)
    1 to < 6 yr (12) 0.869 (0.479) 30.4 (9.16) 61 (10.7)
    6 to < 12 yr (11) 1.12 (0.462) 29.2 (12.6) 66.8 (21.2)
    12 to 18 yr (14) 1.09 (0.518) 18.1 (7.29) 56.7 (14.0)

    The mycophenolate mofetil oral suspension dose of 600 mg/m2 bid (up to a maximum of 1 g bid) achieved mean MPA AUC values in pediatric patients similar to those seen in adult renal transplant patients receiving mycophenolate mofetil capsules at a dose of 1 g bid in the early posttransplant period. There was wide variability in the data. As observed in adults, early posttransplant MPA AUC values were approximately 45% to 53% lower than those observed in the later posttransplant period (> 3 months). MPA AUC values were similar in the early and late posttransplant period across the 1 year to 18 year age range.

    Gender

    Data obtained from several studies were pooled to look at any gender-related differences in the pharmacokinetics of MPA (data were adjusted to 1 g oral dose). Mean (± SD) MPA AUC(0 to 12h) for males (n = 79) was 32 (± 14.5) and for females (n = 41) was 36.5 (± 18.8) mcg•h/mL while mean (± SD) MPA Cmax was 9.96 (± 6.19) in the males and 10.6 (± 5.64) mcg/mL in the females. These differences are not of clinical significance.

    Geriatrics

    Pharmacokinetics in the elderly have not been studied.

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  • CLINICAL STUDIES

    Adults

    The safety and efficacy of mycophenolate mofetil in combination with corticosteroids and cyclosporine for the prevention of organ rejection were assessed in randomized, double-blind, multicenter trials in renal (3 trials), in cardiac (1 trial), and in hepatic (1 trial) adult transplant patients.

    Renal Transplant

    Adults

    The three renal studies compared two dose levels of oral mycophenolate mofetil (1 g bid and 1.5 g bid) with azathioprine (2 studies) or placebo (1 study) when administered in combination with cyclosporine (Sandimmune®) and corticosteroids to prevent acute rejection episodes. One study also included antithymocyte globulin (ATGAM®) induction therapy. These studies are described by geographic location of the investigational sites. One study was conducted in the USA at 14 sites, one study was conducted in Europe at 20 sites, and one study was conducted in Europe, Canada, and Australia at a total of 21 sites.

    The primary efficacy endpoint was the proportion of patients in each treatment group who experienced treatment failure within the first 6 months after transplantation (defined as biopsy-proven acute rejection on treatment or the occurrence of death, graft loss or early termination from the study for any reason without prior biopsy-proven rejection). Mycophenolate mofetil, when administered with antithymocyte globulin (ATGAM®) induction (one study) and with cyclosporine and corticosteroids (all three studies), was compared to the following three therapeutic regimens: (1) antithymocyte globulin (ATGAM®) induction/azathioprine/cyclosporine/corticosteroids, (2) azathioprine/cyclosporine/corticosteroids, and (3) cyclosporine/corticosteroids.

    Mycophenolate mofetil, in combination with corticosteroids and cyclosporine reduced (statistically significant at 0.05 level) the incidence of treatment failure within the first 6 months following transplantation. Table 4 and Table 5 summarize the results of these studies. These tables show (1) the proportion of patients experiencing treatment failure, (2) the proportion of patients who experienced biopsy-proven acute rejection on treatment, and (3) early termination, for any reason other than graft loss or death, without a prior biopsy-proven acute rejection episode. Patients who prematurely discontinued treatment were followed for the occurrence of death or graft loss, and the cumulative incidence of graft loss and patient death are summarized separately. Patients who prematurely discontinued treatment were not followed for the occurrence of acute rejection after termination. More patients receiving mycophenolate mofetil discontinued without prior biopsy-proven rejection, death or graft loss than discontinued in the control groups, with the highest rate in the mycophenolate mofetil 3 g/day group. Therefore, the acute rejection rates may be underestimates, particularly in the mycophenolate mofetil 3 g/day group.

    Table 4: Renal Transplant Studies Incidence of Treatment Failure (Biopsy-Proven Rejection or Early Termination for Any Reason)
    *
    Antithymocyte globulin induction/MMF or azathioprine/cyclosporine/corticosteroids.
    Does not include death and graft loss as reason for early termination.
    MMF or azathioprine/cyclosporine/corticosteroids.
    §
    MMF or placebo/cyclosporine/corticosteroids.
    USAStudy* 
    (N = 499 patients)
    Mycophenolate Mofetil 2 g/day
    (n = 167 patients)
    Mycophenolate Mofetil 3 g/day (n = 166 patients) Azathioprine 1 to 2 mg/kg/day
    (n = 166 patients)
    All treatment failures 31.1% 31.3% 47.6%
    Early termination without prior acute rejection 9.6% 12.7% 6%
    Biopsy-proven rejection episode on treatment 19.8% 17.5% 38%
    Europe/Canada/Australia Study  (N = 503 patients) Mycophenolate Mofetil 2 g/day
    (n = 173 patients)
    Mycophenolate Mofetil 3 g/day (n = 164 patients) Azathioprine 100 to 150 mg/day
    (n = 166 patients)
    All treatment failures 38.2% 34.8% 50%
    Early termination without prior acute rejection 13.9% 15.2% 10.2%
    Biopsy-proven rejection episode on treatment 19.7% 15.9% 35.5%

    Europe Study§ 

    (N = 491 patients)

    Mycophenolate Mofetil 2 g/day

    (n = 165 patients)

    Mycophenolate Mofetil 3 g/day

    (n = 160 patients)

    Placebo

    (n = 166 patients)

    All treatment failures 30.3% 38.8% 56%
    Early termination without prior acute rejection 11.5% 22.5% 7.2%
    Biopsy-proven rejection episode on treatment 17% 13.8% 46.4%

    The cumulative incidence of 12 month graft loss or patient death is presented below. No advantage of mycophenolate mofetil with respect to graft loss or patient death was established. Numerically, patients receiving mycophenolate mofetil 2 g/day and 3 g/day experienced a better outcome than controls in all three studies; patients receiving mycophenolate mofetil 2 g/day experienced a better outcome than mycophenolate mofetil 3 g/day in two of the three studies. Patients in all treatment groups who terminated treatment early were found to have a poor outcome with respect to graft loss or patient death at 1 year.

    Table 5: Renal Transplant Studies Cumulative Incidence of Combined Graft Loss or Patient Death at 12 Months
    Study Mycophenolate Mofetil 2 g/day Mycophenolate Mofetil 3 g/day Control (Azathioprine or Placebo)
    USA 8.5% 11.5% 12.2%
    Europe/Canada/Australia 11.7% 11% 13.6%
    Europe 8.5% 10% 11.5%

    Pediatrics

    One open-label, safety and pharmacokinetic study of mycophenolate mofetil oral suspension 600 mg/m2 bid (up to 1 g bid) in combination with cyclosporine and corticosteroids was performed at centers in the U.S. (9), Europe (5) and Australia (1) in 100 pediatric patients (3 months to 18 years of age) for the prevention of renal allograft rejection. Mycophenolate mofetil was well tolerated in pediatric patients (see ADVERSE REACTIONS), and the pharmacokinetics profile was similar to that seen in adult patients dosed with 1 g bid mycophenolate mofetil capsules (see CLINICAL PHARMACOLOGY,Pharmacokinetics). The rate of biopsy-proven rejection was similar across the age groups (3 months to < 6 years, 6 years to < 12 years, 12 years to 18 years). The overall biopsy-proven rejection rate at 6 months was comparable to adults. The combined incidence of graft loss (5%) and patient death (2%) at 12 months posttransplant was similar to that observed in adult renal transplant patients.

    Cardiac Transplant

    A double-blind, randomized, comparative, parallel-group, multicenter study in primary cardiac transplant recipients was performed at 20 centers in the United States, 1 in Canada, 5 in Europe and 2 in Australia. The total number of patients enrolled was 650; 72 never received study drug and 578 received study drug. Patients received mycophenolate mofetil 1.5 g bid (n = 289) or azathioprine 1.5 to 3 mg/kg/day (n = 289), in combination with cyclosporine (Sandimmune® or Neoral®) and corticosteroids as maintenance immunosuppressive therapy. The two primary efficacy endpoints were: (1) the proportion of patients who, after transplantation, had at least one endomyocardial biopsy-proven rejection with hemodynamic compromise, or were retransplanted or died, within the first 6 months, and (2) the proportion of patients who died or were retransplanted during the first 12 months following transplantation. Patients who prematurely discontinued treatment were followed for the occurrence of allograft rejection for up to 6 months and for the occurrence of death for 1 year.

    (1) Rejection: No difference was established between mycophenolate mofetil and azathioprine (AZA) with respect to biopsy-proven rejection with hemodynamic compromise.

    (2) Survival: Mycophenolate mofetil was shown to be at least as effective as AZA in preventing death or retransplantation at 1 year (see Table 6).

    Table 6: Rejection at 6 Months/Death or Retransplantation at 1 Year
    *
    Hemodynamic compromise occurred if any of the following criteria were met: pulmonary capillary wedge pressure ≥ 20 mm or a 25% increase; cardiac index < 2 L/min/m 2 or a 25% decrease; ejection fraction ≤ 30%; pulmonary artery oxygen saturation ≤ 60% or a 25% decrease; presence of new S 3 gallop; fractional shortening was ≤ 20% or a 25% decrease; inotropic support required to manage the clinical condition.
    All Patients Treated Patients
    AZA
    N
    = 323
    Mycophenolate Mofetil
    N
    = 327
    AZA
    N
    = 289
    Mycophenolate Mofetil
    N
    = 289
    Biopsy-proven rejection with hemodynamic compromise at 6 months* 121 (38%) 120 (37%) 100 (35%) 92 (32%)
    Death or retransplantation at 1 year 49 (15.2%) 42 (12.8%) 33 (11.4%) 18 (6.2%)

    Hepatic Transplant

    A double-blind, randomized, comparative, parallel-group, multicenter study in primary hepatic transplant recipients was performed at 16 centers in the United States, 2 in Canada, 4 in Europe and 1 in Australia. The total number of patients enrolled was 565. Per protocol, patients received mycophenolate mofetil 1 g bid intravenously for up to 14 days followed by mycophenolate mofetil 1.5 g bid orally or azathioprine 1 to 2 mg/kg/day intravenously followed by azathioprine 1 to 2 mg/kg/day orally, in combination with cyclosporine (Neoral®) and corticosteroids as maintenance immunosuppressive therapy. The actual median oral dose of azathioprine on study was 1.5 mg/kg/day (range of 0.3 to 3.8 mg/kg/day) initially and 1.26 mg/kg/day (range of 0.3 to 3.8 mg/kg/day) at 12 months. The two primary endpoints were: (1) the proportion of patients who experienced, in the first 6 months posttransplantation, one or more episodes of biopsy-proven and treated rejection or death or retransplantation, and (2) the proportion of patients who experienced graft loss (death or retransplantation) during the first 12 months posttransplantation. Patients who prematurely discontinued treatment were followed for the occurrence of allograft rejection and for the occurrence of graft loss (death or retransplantation) for 1 year.

    Results

    In combination with corticosteroids and cyclosporine, mycophenolate mofetil obtained a lower rate of acute rejection at 6 months and a similar rate of death or retransplantation at 1 year compared to azathioprine.

    Table 7: Rejection at 6 Months/Death or Retransplantation at 1 Year
    AZA N = 287 Mycophenolate Mofetil N = 278
    Biopsy-proven, treated rejection at 6 months (includes death or retransplantation) 137 (47.7%) 107 (38.5%)
    Death or retransplantation at 1 year 42 (14.6%) 41 (14.7%)
    Close
  • INDICATIONS AND USAGE

    Renal, Cardiac, and Hepatic Transplant

    Mycophenolate mofetil capsules USP and mycophenolate mofetil tablets USP are indicated for the prophylaxis of organ rejection in patients receiving allogeneic renal, cardiac or hepatic transplants. Mycophenolate mofetil, USP should be used concomitantly with cyclosporine and corticosteroids.

    Close
  • CONTRAINDICATIONS

    Allergic reactions to mycophenolate mofetil have been observed; therefore, mycophenolate mofetil capsules and mycophenolate mofetil tablets are contraindicated in patients with a hypersensitivity to mycophenolate mofetil, mycophenolic acid or any component of the drug product.

    Close
  • WARNINGS

    (See boxed WARNING.)

    Embryofetal Toxicity

    Mycophenolate mofetil (MMF) can cause fetal harm when administered to a pregnant

    female. Use of MMF during pregnancy is associated with an increased risk of first

    trimester pregnancy loss and an increased risk of congenital malformations, especially

    external ear and other facial abnormalities including cleft lip and palate, and anomalies of

    the distal limbs, heart, esophagus, and kidney (see PRECAUTIONS, Pregnancy).

    Pregnancy Exposure Prevention and Planning

    Females of reproductive potential must be made aware of the increased risk of first

    trimester pregnancy loss and congenital malformations and must be counseled regarding

    pregnancy prevention and planning. For recommended pregnancy testing and

    contraception methods (see PRECAUTIONS, Pregnancy Exposure Prevention and Planning).

    Lymphoma and Malignancy

    Patients receiving immunosuppressive regimens involving combinations of drugs, including mycophenolate mofetil, as part of an immunosuppressive regimen are at increased risk of developing lymphomas and other malignancies, particularly of the skin (see ADVERSE REACTIONS). The risk appears to be related to the intensity and duration of immunosuppression rather than to the use of any specific agent.

    As usual for patients with increased risk for skin cancer, exposure to sunlight and UV light should be limited by wearing protective clothing and using a sunscreen with a high protection factor.

    Lymphoproliferative disease or lymphoma developed in 0.4% to 1% of patients receiving mycophenolate mofetil (2 g or 3 g) with other immunosuppressive agents in controlled clinical trials of renal, cardiac, and hepatic transplant patients (see ADVERSE REACTIONS).

    In pediatric patients, no other malignancies besides lymphoproliferative disorder (2/148 patients) have been observed (see ADVERSE REACTIONS).

    Combination With Other Immunosuppressive Agents

    Mycophenolate mofetil has been administered in combination with the following agents in clinical trials: antithymocyte globulin (ATGAM®), OKT3 (Orthoclone OKT® 3), cyclosporine (Sandimmune®, Neoral®) and corticosteroids. The efficacy and safety of the use of mycophenolate mofetil in combination with other immunosuppressive agents have not been determined.

    Serious Infections

    Patients receiving immunosuppressants, including mycophenolate mofetil, are at increased risk of developing bacterial, fungal, protozoal and new or reactivated viral infections, including opportunistic infections. These infections may lead to serious, including fatal outcomes. Because of the danger of oversuppression of the immune system which can increase susceptibility to infection, combination immunosuppressant therapy should be used with caution (see ADVERSE REACTIONS).

    New or Reactivated Viral Infections

    Polyomavirus associated nephropathy (PVAN), JC virus associated progressive multifocal leukoencephalopathy (PML), cytomegalovirus (CMV) infections, reactivation of hepatitis B (HBV) or hepatitis C (HCV) have been reported in patients treated with immunosuppressants, including mycophenolate mofetil. Reduction in immunosuppression should be considered for patients who develop evidence of new or reactivated viral infections. Physicians should also consider the risk that reduced immunosuppression represents to the functioning allograft.

    PVAN, especially due to BK virus infection, is associated with serious outcomes, including deteriorating renal function and renal graft loss (see ADVERSE REACTIONS, Postmarketing Experience). Patient monitoring may help detect patients at risk for PVAN.

    PML, which is sometimes fatal, commonly presents with hemiparesis, apathy, confusion, cognitive deficiencies, and ataxia. Risk factors for PML include treatment with immunosuppressant therapies and impairment of immune function (see ADVERSE REACTIONS, Postmarketing Experience). In immunosuppressed patients, physicians should consider PML in the differential diagnosis in patients reporting neurological symptoms and consultation with a neurologist should be considered as clinically indicated.

    The risk of CMV viremia and CMV disease is highest among transplant recipients seronegative for CMV at time of transplant who receive a graft from a CMV seropositive donor. Therapeutic approaches to limiting CMV disease exist and should be routinely provided. Patient monitoring may help detect patients at risk for CMV disease.

    Viral reactivation has been reported in patients infected with HBV or HCV. Monitoring infected patients for clinical and laboratory signs of active HBV or HCV infection is recommended.

    Neutropenia

    Severe neutropenia [absolute neutrophil count (ANC) < 0.5 x 103/µL] developed in up to 2.0% of renal, up to 2.8% of cardiac, and up to 3.6% of hepatic transplant patients receiving mycophenolate mofetil 3 g daily (see ADVERSE REACTIONS). Patients receiving mycophenolate mofetil should be monitored for neutropenia (see PRECAUTIONS, Laboratory Tests). The development of neutropenia may be related to mycophenolate mofetil itself, concomitant medications, viral infections, or some combination of these causes. If neutropenia develops (ANC < 1.3 x 103/µL), dosing with mycophenolate mofetil should be interrupted or the dose reduced, appropriate diagnostic tests performed, and the patient managed appropriately (see DOSAGE AND ADMINISTRATION). Neutropenia has been observed most frequently in the period from 31 to 180 days posttransplant in patients treated for prevention of renal, cardiac, and hepatic rejection.

    Patients receiving mycophenolate mofetil should be instructed to report immediately any evidence of infection, unexpected bruising, bleeding or any other manifestation of bone marrow depression.

    Pure Red Cell Aplasia (PRCA)

    Cases of pure red cell aplasia (PRCA) have been reported in patients treated with mycophenolate mofetil in combination with other immunosuppressive agents. The mechanism for mycophenolate mofetil induced PRCA is unknown; the relative contribution of other immunosuppressants and their combinations in an immunosuppression regimen are also unknown. In some cases, PRCA was found to be reversible with dose reduction or cessation of mycophenolate mofetil therapy. In transplant patients, however, reduced immunosuppression may place the graft at risk.

    Close
  • PRECAUTIONS

    Pregnancy Exposure Prevention and Planning

    Females of reproductive potential must be made aware of the increased risk of first

    trimester pregnancy loss and congenital malformations and must be counseled regarding

    pregnancy prevention and planning.

    Females of reproductive potential include girls who have entered puberty and all women

    who have a uterus and have not passed through menopause. Menopause is the permanent

    end of menstruation and fertility. Menopause should be clinically confirmed by a

    patient’s healthcare practitioner. Some commonly used diagnostic criteria include 1) 12

    months of spontaneous amenorrhea (not amenorrhea induced by a medical condition or

    medical therapy) or 2) postsurgical from a bilateral oophorectomy.

    Pregnancy Testing

    To prevent unplanned exposure during pregnancy, females of reproductive potential should have a serum or urine pregnancy test with a sensitivity of at least 25 mIU/mL immediately before starting mycophenolate mofetil. Another pregnancy test with the same sensitivity should be done 8 to 10 days later. Repeat pregnancy tests should be performed during routine follow-up visits. Results of all pregnancy tests should be discussed with the patient.

    In the event of a positive pregnancy test, females should be counseled with regard to whether the maternal benefits of mycophenolate treatment may outweigh the risks to the fetus in certain situations.

    Contraception

    Females of reproductive potential taking mycophenolate mofetil must receive contraceptive counseling and use acceptable contraception (see Table 8 for acceptable contraception methods).

    Patients must use acceptable birth control during entire mycophenolate mofetil therapy, and for 6 weeks after stopping mycophenolate mofetil, unless the patient chooses abstinence (she chooses to avoid heterosexual intercourse completely).

    Patients should be aware that mycophenolate mofetil reduces blood levels of the hormones in the oral contraceptive pill and could theoretically reduce its effectiveness (see PRECAUTIONS,

    Information for Patientsand PRECAUTIONS, Drug Interactions,  

    Oral Contraceptives).

    Table 8: Acceptable Contraception Methods for Females of Reproductive Potential Pick from the following birth control options:

    Option 1

     

    Methods to

    Use Alone
    • Intrauterine devices (IUDs)
    • Tubal sterilization
    • Patient's partner had a vasectomy

    OR

    Option 2

    Hormone Methods

    Choose 1

    Barrier Methods

    Choose 1

    Choose One

    Hormone

    Method AND

    One Barrier

    Method

    Estrogen and Progesterone

    • Oral Contraceptive Pill
    • Transdermal patch
    • Vaginal ring

    Progesterone-only

    • Injection
    • Implant
    AND
    • Diaphragm with spermicide
    • Cervical cap with spermicide
    • Contraceptive sponge
    • Male condom
    • Female condom
     

    OR

    Option 3

    Barrier Methods

    Choose 1

    Barrier Methods

    Choose 1

    Choose One Barrier

    Method From Each Column(must choose two methods)
    • Diaphragm with spermicide
    • Cervical cap with spermicide
    • Contraceptive sponge
    AND
    • Male condom
    • Female condom
     

    Pregnancy Planning

    For patients who are considering pregnancy, consider alternative immunosuppressants with less potential for embryofetal toxicity. Risks and benefits of mycophenolate mofetil should be discussed with the patient.

    Gastrointestinal Disorders

    Gastrointestinal bleeding (requiring hospitalization) has been observed in approximately 3% of renal, in 1.7% of cardiac, and in 5.4% of hepatic transplant patients treated with mycophenolate mofetil 3 g daily. In pediatric renal transplant patients, 5/148 cases of gastrointestinal bleeding (requiring hospitalization) were observed.

    Gastrointestinal perforations have rarely been observed. Most patients receiving mycophenolate mofetil were also receiving other drugs known to be associated with these complications. Patients with active peptic ulcer disease were excluded from enrollment in studies with mycophenolate mofetil. Because mycophenolate mofetil has been associated with an increased incidence of digestive system adverse events, including infrequent cases of gastrointestinal tract ulceration, hemorrhage, and perforation, mycophenolate mofetil should be administered with caution in patients with active serious digestive system disease.

    Patients With Renal Impairment

    Subjects with severe chronic renal impairment (GFR < 25 mL/min/1.73 m2) who have received single doses of mycophenolate mofetil showed higher plasma MPA and MPAG AUCs relative to subjects with lesser degrees of renal impairment or normal healthy volunteers. No data are available on the safety of long-term exposure to these levels of MPAG. Doses of mycophenolate mofetil greater than 1 g administered twice a day to renal transplant patients should be avoided and they should be carefully observed (see CLINICAL PHARMACOLOGY, Pharmacokineticsand DOSAGE AND ADMINISTRATION).

    No data are available for cardiac or hepatic transplant patients with severe chronic renal impairment. Mycophenolate mofetil may be used for cardiac or hepatic transplant patients with severe chronic renal impairment if the potential benefits outweigh the potential risks.

    In patients with delayed renal graft function posttransplant, mean MPA AUC(0 to12h) was comparable, but MPAG AUC(0 to12h) was 2 fold to 3 fold higher, compared to that seen in posttransplant patients without delayed renal graft function. In the three controlled studies of prevention of renal rejection, there were 298 of 1483 patients (20%) with delayed graft function. Although patients with delayed graft function have a higher incidence of certain adverse events (anemia, thrombocytopenia, hyperkalemia) than patients without delayed graft function, these events were not more frequent in patients receiving mycophenolate mofetil than azathioprine or placebo. No dose adjustment is recommended for these patients; however, they should be carefully observed (see CLINICAL PHARMACOLOGY, Pharmacokineticsand DOSAGE AND ADMINISTRATION).

    Infections in Cardiac Transplant Patients

    In cardiac transplant patients, the overall incidence of opportunistic infections was approximately 10% higher in patients treated with mycophenolate mofetil than in those receiving azathioprine therapy, but this difference was not associated with excess mortality due to infection/sepsis among patients treated with mycophenolate mofetil (see ADVERSE REACTIONS).

    There were more herpes virus (H. simplex, H. zoster, and cytomegalovirus) infections in cardiac transplant patients treated with mycophenolate mofetil compared to those treated with azathioprine (see ADVERSE REACTIONS).

    Concomitant Medications

    It is recommended that mycophenolate mofetil not be administered concomitantly with azathioprine because both have the potential to cause bone marrow suppression and such concomitant administration has not been studied clinically.

    In view of the significant reduction in the AUC of MPA by cholestyramine, caution should be used in the concomitant administration of mycophenolate mofetil with drugs that interfere with enterohepatic recirculation because of the potential to reduce the efficacy of mycophenolate mofetil (see PRECAUTIONS, Drug Interactions).

    Patients With HGPRT Deficiency

    On theoretical grounds, because mycophenolate mofetil is an IMPDH (inosine monophosphate dehydrogenase) inhibitor, it should be avoided in patients with rare hereditary deficiency of hypoxanthine-guanine phosphoribosyl-transferase (HGPRT) such as Lesch-Nyhan and Kelley-Seegmiller syndrome.

    Immunizations

    During treatment with mycophenolate mofetil, the use of live attenuated vaccines should be avoided and patients should be advised that vaccinations may be less effective (see PRECAUTIONS, Drug Interactions, Live Vaccines).

    Phenylketonurics

    Mycophenolate mofetil oral suspension contains aspartame, a source of phenylalanine (0.56 mg phenylalanine/mL suspension). Therefore, care should be taken if mycophenolate mofetil oral suspension is administered to patients with phenylketonuria.

    Information for Patients

    • See Medication Guide

    • Inform females of reproductive potential that use of mycophenolate mofetil during pregnancy is associated with an increased risk of first trimester pregnancy loss and an increased risk of congenital malformations, and advise them as to the appropriate steps to manage these risks, including that they must use acceptable contraception (see WARNINGS, Embryofetal Toxicity; PRECAUTIONS, Pregnancy Exposure Prevention and Planning).
    • Discuss pregnancy testing, pregnancy prevention and planning with females of reproductive potential. In the event of a positive pregnancy test, females should be counseled with regard to whether the maternal benefits of mycophenolate treatment may outweigh the risks to the fetus in certain situations.
    • Females of reproductive potential must use acceptable birth control during entire mycophenolate mofetil therapy and for 6 weeks after stopping mycophenolate mofetil, unless the patient chooses to avoid heterosexual intercourse completely (abstinence) (see PRECAUTIONS, Pregnancy Exposure Prevention and Planning, Table 8).
    • For patients who are considering pregnancy, discuss appropriate alternative immunosuppressants with less potential for embryofetal toxicity. Risks and benefits of mycophenolate mofetil should be discussed with the patient.
    • Give patients complete dosage instructions and inform them about the increased risk of lymphoproliferative disease and certain other malignancies.
    • Inform patients that they need repeated appropriate laboratory tests while they are taking mycophenolate mofetil.
    • Advise patients that they should not breastfeed during mycophenolate mofetil therapy.

    Laboratory Tests

    Complete blood counts should be performed weekly during the first month, twice monthly for the second and third months of treatment, then monthly through the first year (see WARNINGS, ADVERSE REACTIONS, andDOSAGE AND ADMINISTRATION).

    Drug Interactions

    Drug interaction studies with mycophenolate mofetil have been conducted with acyclovir, antacids, cholestyramine, cyclosporine, ganciclovir, oral contraceptives, sevelamer, trimethoprim/sulfamethoxazole, norfloxacin, and metronidazole. Drug interaction studies have not been conducted with other drugs that may be commonly administered to renal, cardiac or hepatic transplant patients. Mycophenolate mofetil has not been administered concomitantly with azathioprine.

    Acyclovir

    Coadministration of mycophenolate mofetil (1 g) and acyclovir (800 mg) to 12 healthy volunteers resulted in no significant change in MPA AUC and Cmax. However, MPAG and acyclovir plasma AUCs were increased 10.6% and 21.9%, respectively. Because MPAG plasma concentrations are increased in the presence of renal impairment, as are acyclovir concentrations, the potential exists for mycophenolate and acyclovir or its prodrug (e.g., valacyclovir) to compete for tubular secretion, further increasing the concentrations of both drugs.

    Antacids With Magnesium and Aluminum Hydroxides

    Absorption of a single dose of mycophenolate mofetil (2 g) was decreased when administered to ten rheumatoid arthritis patients also taking Maalox® TC (10 mL qid). The Cmax and AUC(0 to 24h) for MPA were 33% and 17% lower, respectively, than when mycophenolate mofetil was administered alone under fasting conditions. Mycophenolate mofetil may be administered to patients who are also taking antacids containing magnesium and aluminum hydroxides; however, it is recommended that mycophenolate mofetil and the antacid not be administered simultaneously.

    Proton Pump Inhibitors (PPIs)

    Coadministration of PPIs (e.g., lansoprazole, pantoprazole) in single doses to healthy volunteers and multiple doses to transplant patients receiving mycophenolate mofetil has been reported to reduce the exposure to mycophenolic acid (MPA). An approximate reduction of 30 to 70% in the Cmax and 25% to 35% in the AUC of MPA has been observed, possibly due to a decrease in MPA solubility at an increased gastric pH. The clinical impact of reduced MPA exposure on organ rejection has not been established in transplant patients receiving PPIs and mycophenolate mofetil. Because clinical relevance has not been established, PPIs should be used with caution when coadministered to transplant patients being treated with mycophenolate mofetil.

    Cholestyramine

    Following single-dose administration of 1.5 g mycophenolate mofetil to 12 healthy volunteers pretreated with 4 g tid of cholestyramine for 4 days, MPA AUC decreased approximately 40%. This decrease is consistent with interruption of enterohepatic recirculation which may be due to binding of recirculating MPAG with cholestyramine in the intestine. Some degree of enterohepatic recirculation is also anticipated following intravenous administration of mycophenolate mofetil. Therefore, mycophenolate mofetil is not recommended to be given with cholestyramine or other agents that may interfere with enterohepatic recirculation.

    Cyclosporine

    Cyclosporine (Sandimmune®) pharmacokinetics (at doses of 275 to 415 mg/day) were unaffected by single and multiple doses of 1.5 g bid of mycophenolate mofetil in 10 stable renal transplant patients. The mean (± SD) AUC(0 to 12h) and Cmax of cyclosporine after 14 days of multiple doses of mycophenolate mofetil were 3290 (± 822) ng•h/mL and 753 (± 161) ng/mL, respectively, compared to 3245 (± 1088) ng•h/mL and 700 (± 246) ng/mL, respectively, 1 week before administration of mycophenolate mofetil.

    In renal transplant patients, mean MPA exposure (AUC0 to 12h) was approximately 30 to 50% greater when mycophenolate mofetil is administered without cyclosporine compared with when mycophenolate mofetil is coadministered with cyclosporine. This interaction is due to cyclosporine inhibition of multidrug-resistance-associated protein 2 (MRP-2) transporter in the biliary tract, thereby preventing the excretion of MPAG into the bile that would lead to enterohepatic recirculation of MPA. This information should be taken into consideration when MMF is used without cyclosporine.

    Ganciclovir

    Following single-dose administration to 12 stable renal transplant patients, no pharmacokinetic interaction was observed between mycophenolate mofetil (1.5 g) and intravenous ganciclovir (5 mg/kg). Mean (± SD) ganciclovir AUC and Cmax (n = 10) were 54.3 (± 19) mcg•h/mL and 11.5 (± 1.8) mcg/mL, respectively, after coadministration of the two drugs, compared to 51 (± 17) mcg•h/mL and 10.6 (± 2) mcg/mL, respectively, after administration of intravenous ganciclovir alone. The mean (± SD) AUC and Cmax of MPA (n = 12) after coadministration were 80.9 (± 21.6) mcg•h/mL and 27.8 (± 13.9) mcg/mL, respectively, compared to values of 80.3 (± 16.4) mcg•h/mL and 30.9 (± 11.2) mcg/mL, respectively, after administration of mycophenolate mofetil alone. Because MPAG plasma concentrations are increased in the presence of renal impairment, as are ganciclovir concentrations, the two drugs will compete for tubular secretion and thus further increases in concentrations of both drugs may occur. In patients with renal impairment in which MMF and ganciclovir or its prodrug (e.g., valganciclovir) are coadministered, patients should be monitored carefully.

    Oral Contraceptives

    A study of coadministration of mycophenolate mofetil (1 g bid) and combined oral contraceptives containing ethinylestradiol (0.02 mg to 0.04 mg) and levonorgestrel (0.05 mg to 0.20 mg), desogestrel (0.15 mg) or gestodene (0.05 mg to 0.10 mg) was conducted in 18 women with psoriasis over 3 consecutive menstrual cycles. Mean AUC(0 to 24h) was similar for ethinylestradiol and 3-keto desogestrel; however, mean levonorgestrel AUC(0 to 24h) significantly decreased by about 15%. There was large inter-patient variability (% CV in the range of 60% to 70%) in the data, especially for ethinylestradiol. Mean serum levels of LH, FSH and progesterone were not significantly affected. Mycophenolate mofetil may not have any influence on the ovulation-suppressing action of the studied oral contraceptives. It is recommended to coadminister mycophenolate mofetil with hormonal contraceptives (e.g., birth control pill, transdermal patch, vaginal ring, injection, and implant) with caution and additional barrier contraceptive methods must be used (see PRECAUTIONS, Pregnancy Exposure Prevention and Planning).

    Sevelamer

    Concomitant administration of sevelamer and mycophenolate mofetil in adult and pediatric patients decreased the mean MPA Cmax and AUC0 to 12h by 36% and 26% respectively. This data suggest that sevelamer and other calcium free phosphate binders should not be administered simultaneously with mycophenolate mofetil. Alternatively, it is recommended that sevelamer and other calcium free phosphate binders preferentially could be given 2 hours after mycophenolate mofetil intake to minimize the impact on the absorption of MPA.

    Trimethoprim/Sulfamethoxazole

    Following single-dose administration of mycophenolate mofetil (1.5 g) to 12 healthy male volunteers on day 8 of a 10 day course of trimethoprim 160 mg/sulfamethoxazole 800 mg administered bid, no effect on the bioavailability of MPA was observed. The mean (± SD) AUC and Cmax of MPA after concomitant administration were 75.2 (± 19.8) mcg•h/mL and 34 (± 6.6) mcg/mL, respectively, compared to 79.2 (± 27.9) mcg•h/mL and 34.2 (± 10.7) mcg/mL, respectively, after administration of mycophenolate mofetil alone.

    Norfloxacin and Metronidazole

    Following single-dose administration of mycophenolate mofetil (1 g) to 11 healthy volunteers on day 4 of a 5 day course of a combination of norfloxacin and metronidazole, the mean MPA AUC0 to 48h was significantly reduced by 33% compared to the administration of mycophenolate mofetil alone (p < 0.05). Therefore, mycophenolate mofetil is not recommended to be given with the combination of norfloxacin and metronidazole. There was no significant effect on mean MPA AUC0 to 48h when mycophenolate mofetil was concomitantly administered with norfloxacin or metronidazole separately. The mean (± SD) MPA AUC0 to 48h after coadministration of mycophenolate mofetil with norfloxacin or metronidazole separately was 48.3 (± 24) mcg•h/mL and 42.7 (± 23) mcg•h/mL, respectively, compared with 56.2 (± 24) mcg•h/mL after administration of mycophenolate mofetil alone.

    Ciprofloxacin and Amoxicillin Plus Clavulanic Acid

    A total of 64 mycophenolate mofetil-treated renal transplant recipients received either oral ciprofloxacin 500 mg bid or amoxicillin plus clavulanic acid 375 mg tid for 7 or at least 14 days. Approximately 50% reductions in median trough MPA concentrations (pre-dose) from baseline (mycophenolate mofetil alone) were observed in 3 days following commencement of oral ciprofloxacin or amoxicillin plus clavulanic acid. These reductions in trough MPA concentrations tended to diminish within 14 days of antibiotic therapy and ceased within 3 days after discontinuation of antibiotics. The postulated mechanism for this interaction is an antibiotic-induced reduction in glucuronidase-possessing enteric organisms leading to a decrease in enterohepatic recirculation of MPA. The change in trough level may not accurately represent changes in overall MPA exposure; therefore, clinical relevance of these observations is unclear.

    Rifampin

    In a single heart-lung transplant patient, after correction for dose, a 67% decrease in MPA exposure (AUC0 to 12h) has been observed with concomitant administration of mycophenolate mofetil and rifampin. Therefore, mycophenolate mofetil is not recommended to be given with rifampin concomitantly unless the benefit outweighs the risk.

    Other Interactions

    The measured value for renal clearance of MPAG indicates removal occurs by renal tubular secretion as well as glomerular filtration. Consistent with this, coadministration of probenecid, a known inhibitor of tubular secretion, with mycophenolate mofetil in monkeys results in a 3 fold increase in plasma MPAG AUC and a 2 fold increase in plasma MPA AUC. Thus, other drugs known to undergo renal tubular secretion may compete with MPAG and thereby raise plasma concentrations of MPAG or the other drug undergoing tubular secretion.

    Drugs that alter the gastrointestinal flora may interact with mycophenolate mofetil by disrupting enterohepatic recirculation. Interference of MPAG hydrolysis may lead to less MPA available for absorption.

    Live Vaccines

    During treatment with mycophenolate mofetil, the use of live attenuated vaccines should be avoided and patients should be advised that vaccinations may be less effective (see PRECAUTIONS,Immunizations). Influenza vaccination may be of value. Prescribers should refer to national guidelines for influenza vaccination.

    Carcinogenesis, Mutagenesis, Impairment of Fertility

    In a 104 week oral carcinogenicity study in mice, mycophenolate mofetil in daily doses up to 180 mg/kg was not tumorigenic. The highest dose tested was 0.5 times the recommended clinical dose (2 g/day) in renal transplant patients and 0.3 times the recommended clinical dose (3 g/day) in cardiac transplant patients when corrected for differences in body surface area (BSA). In a 104 week oral carcinogenicity study in rats, mycophenolate mofetil in daily doses up to 15 mg/kg was not tumorigenic. The highest dose was 0.08 times the recommended clinical dose in renal transplant patients and 0.05 times the recommended clinical dose in cardiac transplant patients when corrected for BSA. While these animal doses were lower than those given to patients, they were maximal in those species and were considered adequate to evaluate the potential for human risk (see WARNINGS).

    The genotoxic potential of mycophenolate mofetil was determined in five assays. Mycophenolate mofetil was genotoxic in the mouse lymphoma/thymidine kinase assay and the in vivo mouse micronucleus assay. Mycophenolate mofetil was not genotoxic in the bacterial mutation assay, the yeast mitotic gene conversion assay or the Chinese hamster ovary cell chromosomal aberration assay.

    Mycophenolate mofetil had no effect on fertility of male rats at oral doses up to 20 mg/kg/day. This dose represents 0.1 times the recommended clinical dose in renal transplant patients and 0.07 times the recommended clinical dose in cardiac transplant patients when corrected for BSA. In a female fertility and reproduction study conducted in rats, oral doses of 4.5 mg/kg/day caused malformations (principally of the head and eyes) in the first generation offspring in the absence of maternal toxicity. This dose was 0.02 times the recommended clinical dose in renal transplant patients and 0.01 times the recommended clinical dose in cardiac transplant patients when corrected for BSA. No effects on fertility or reproductive parameters were evident in the dams or in the subsequent generation.

    Pregnancy

    Teratogenic Effects

    Pregnancy Category D

    See WARNINGS section.

    Use of MMF during pregnancy is associated with an increased risk of first trimester pregnancy loss and an increased risk of congenital malformations, especially external ear and other facial abnormalities including cleft lip and palate, and anomalies of the distal limbs, heart, esophagus, and kidney. In animal studies, congenital malformations and pregnancy loss occurred when pregnant rats and rabbits received mycophenolic acid at dose multiples similar to and less than clinical doses. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to the fetus.

    Risks and benefits of mycophenolate mofetil should be discussed with the patient. When appropriate, consider alternative immunosuppressants with less potential for embryofetal toxicity. In certain situations, the patient and her healthcare practitioner may decide that the maternal benefits outweigh the risks to the fetus. For those females using mycophenolate mofetil at any time during pregnancy and those becoming pregnant within 6 weeks of discontinuing therapy, the healthcare practitioner should report the pregnancy to the Mycophenolate Pregnancy Registry (1-800-617-8191). The healthcare practitioner should strongly encourage the patient to enroll in the pregnancy registry. The information provided to the registry will help the healthcare community better understand the effects of mycophenolate in pregnancy.

    In the National Transplantation Pregnancy Registry (NTPR), there were data on 33 MMF-exposed pregnancies in 24 transplant patients; there were 15 spontaneous abortions (45%) and 18 live-born infants. Four of these 18 infants had structural malformations (22%). In postmarketing data (collected 1995 to 2007) on 77 females exposed to systemic MMF during pregnancy, 25 had spontaneous abortions and 14 had a malformed infant or fetus. Six of 14 malformed offspring had ear abnormalities. Because these postmarketing data are reported voluntarily, it is not always possible to reliably estimate the frequency of particular adverse outcomes. These malformations are similar to findings in animal reproductive toxicology studies. For comparison, the background rate for congenital anomalies in the United States is about 3%, and NTPR data show a rate of 4 to 5% among babies born to organ transplant patients using other immunosuppressive drugs.

    In animal reproductive toxicology studies, there were increased rates of fetal resorptions and malformations in the absence of maternal toxicity. Female rats and rabbits received mycophenolate mofetil (MMF) doses equivalent to 0.02 to 0.9 times the recommended human dose for renal and cardiac transplant patients, based on body surface area conversions. In rat offspring, malformations included anophthalmia, agnathia, and hydrocephaly. In rabbit offspring, malformations included ectopia cordis, ectopic kidneys, diaphragmatic hernia, and umbilical hernia.

    Nursing Mothers

    Studies in rats treated with mycophenolate mofetil have shown mycophenolic acid to be excreted in milk. It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, and because of the potential for serious adverse reactions in nursing infants from mycophenolate mofetil, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

    Pediatric Use

    Based on pharmacokinetic and safety data in pediatric patients after renal transplantation, the recommended dose of mycophenolate mofetil oral suspension is 600 mg/m2 bid (up to a maximum of 1 g bid). Also see CLINICAL PHARMACOLOGY, CLINICAL STUDIES, ADVERSE REACTIONS, andDOSAGE AND ADMINISTRATION.

    Safety and effectiveness in pediatric patients receiving allogeneic cardiac or hepatic transplants have not been established.

    Geriatric Use

    Clinical studies of mycophenolate mofetil did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. In general dose selection for an elderly patient should be cautious, reflecting the greater frequency of decreased hepatic, renal or cardiac function and of concomitant or other drug therapy. Elderly patients may be at an increased risk of adverse reactions compared with younger individuals (see ADVERSE REACTIONS).

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  • ADVERSE REACTIONS

    The principal adverse reactions associated with the administration of mycophenolate mofetil include diarrhea, leukopenia, sepsis, vomiting, and there is evidence of a higher frequency of certain types of infections, e.g., opportunistic infection (see WARNINGS, Serious Infections and WARNINGS, New or Reactivated Viral Infections). The adverse event profile associated with the administration of mycophenolate mofetil intravenous has been shown to be similar to that observed after administration of oral dosage forms of mycophenolate mofetil.

    Mycophenolate Mofetil Oral

    The incidence of adverse events for mycophenolate mofetil was determined in randomized, comparative, double-blind trials in prevention of rejection in renal (2 active, 1 placebo-controlled trials), cardiac (1 active-controlled trial), and hepatic (1 active-controlled trial) transplant patients.

    Geriatrics

    Elderly patients (≥ 65 years), particularly those who are receiving mycophenolate mofetil as part of a combination immunosuppressive regimen, may be at increased risk of certain infections (including cytomegalovirus [CMV] tissue invasive disease) and possibly gastrointestinal hemorrhage and pulmonary edema, compared to younger individuals (see PRECAUTIONS).

    Safety data are summarized below for all active-controlled trials in renal (2 trials), cardiac (1 trial), and hepatic (1 trial) transplant patients. Approximately 53% of the renal patients, 65% of the cardiac patients, and 48% of the hepatic patients have been treated for more than 1 year. Adverse events reported in ≥ 20% of patients in the mycophenolate mofetil treatment groups are presented below.

    Table 9: Adverse Events in Controlled Studies in Prevention of Renal, Cardiac or Hepatic Allograft Rejection (Reported in ≥ 20% of Patients in the Mycophenolate Mofetil Group)
    Renal Studies Cardiac Study Hepatic Study
    Mycophenolate Mofetil 2 g/day Mycophenolate Mofetil 3 g/day Azathioprine 1 to 2 mg/kg/day or 100 to 150 mg/day Mycophenolate Mofetil 3 g/day Azathioprine 1.5 to 3 mg/kg/day Mycophenolate Mofetil 3 g/day Azathioprine 1 to 2 mg/kg/day
    (n = 336) (n = 330) (n = 326) (n = 289) (n = 289) (n = 277) (n = 287)
    % % % % % % %
    Body as a Whole
    Pain 33 31.2 32.2 75.8 74.7 74 77.7
    Abdominal pain 24.7 27.6 23 33.9 33.2 62.5 51.2
    Fever 21.4 23.3 23.3 47.4 46.4 52.3 56.1
    Headache 21.1 16.1 21.2 54.3 51.9 53.8 49.1
    Infection 18.2 20.9 19.9 25.6 19.4 27.1 25.1
    Sepsis 27.4 26.5
    Asthenia 43.3 36.3 35.4 33.8
    Chest pain 26.3 26
    Back pain 34.6 28.4 46.6 47.4
    Ascites 24.2 22.6
    Hematologic and Lymphatic
    Anemia 25.6 25.8 23.6 42.9 43.9 43 53
    Leukopenia 23.2 34.5 24.8 30.4 39.1 45.8 39
    Thrombocytopenia 23.5 27 38.3 42.2
    Hypochromic anemia 24.6 23.5
    Leukocytosis 40.5 35.6 22.4 21.3
    Urogenital
    Urinary tract infection 37.2 37 33.7
    Kidney function abnormal 21.8 26.3 25.6 28.9
    Cardiovascular
    Hypertension 32.4 28.2 32.2 77.5 72.3 62.1 59.6
    Hypotension 32.5 36
    Cardiovascular disorder 25.6 24.2
    Tachycardia 20.1 18 22 15.7
    Metabolic and Nutritional
    Peripheral edema 28.6 27 28.2 64 53.3 48.4 47.7
    Hyper-cholesteremia 41.2 38.4
    Edema 26.6 25.6 28.2 28.2
    Hypokalemia 31.8 25.6 37.2 41.1
    Hyperkalemia 22 23.7
    Hyperglycemia 46.7 52.6 43.7 48.8
    Creatinine increased 39.4 36
    BUN increased 34.6 32.5
    Lactic dehydrogenase increased 23.2 17
    Hypomagnesemia 39 37.6
    Hypocalcemia 30 30
    Digestive
    Diarrhea 31 36.1 20.9 45.3 34.3 51.3 49.8
    Constipation 22.9 18.5 22.4 41.2 37.7 37.9 38.3
    Nausea 19.9 23.6 24.5 54 54.3 54.5 51.2
    Dyspepsia 22.4 20.9
    Vomiting 33.9 28.4 32.9 33.4
    Anorexia 25.3 17.1
    Liver function tests abnormal 24.9 19.2
    Respiratory
    Infection 22 23.9 19.6 37 35.3
    Dyspnea 36.7 36.3 31 30.3
    Cough increased 31.1 25.6
    Lung disorder 30.1 29.1 22 18.8
    Sinusitis 26 19
    Pleural effusion 34.3 35.9
    Skin and Appendages
    Rash 22.1 18
    Nervous System
    Tremor 24.2 23.9 33.9 35.5
    Insomnia 40.8 37.7 52.3 47
    Dizziness 28.7 27.7
    Anxiety 28.4 23.9
    Paresthesia 20.8 18

    The placebo-controlled renal transplant study generally showed fewer adverse events occurring in ≥ 20% of patients. In addition, those that occurred were not only qualitatively similar to the azathioprine-controlled renal transplant studies, but also occurred at lower rates, particularly for infection, leukopenia, hypertension, diarrhea and respiratory infection.

    The above data demonstrate that in three controlled trials for prevention of renal rejection, patients receiving 2 g/day of mycophenolate mofetil had an overall better safety profile than did patients receiving 3 g/day of mycophenolate mofetil.

    The above data demonstrate that the types of adverse events observed in multicenter controlled trials in renal, cardiac, and hepatic transplant patients are qualitatively similar except for those that are unique to the specific organ involved.

    Sepsis, which was generally CMV viremia, was slightly more common in renal transplant patients treated with mycophenolate mofetil compared to patients treated with azathioprine. The incidence of sepsis was comparable in mycophenolate mofetil and in azathioprine-treated patients in cardiac and hepatic studies.

    In the digestive system, diarrhea was increased in renal and cardiac transplant patients receiving mycophenolate mofetil compared to patients receiving azathioprine, but was comparable in hepatic transplant patients treated with mycophenolate mofetil or azathioprine.

    Patients receiving mycophenolate mofetil alone or as part of an immunosuppressive regimen are at increased risk of developing lymphomas and other malignancies, particularly of the skin (see WARNINGS, Lymphoma and Malignancy). The incidence of malignancies among the 1483 patients treated in controlled trials for the prevention of renal allograft rejection who were followed for ≥ 1 year was similar to the incidence reported in the literature for renal allograft recipients.

    Lymphoproliferative disease or lymphoma developed in 0.4% to 1% of patients receiving mycophenolate mofetil (2 g or 3 g daily) with other immunosuppressive agents in controlled clinical trials of renal, cardiac, and hepatic transplant patients followed for at least 1 year (see WARNINGS, Lymphoma and Malignancy). Non-melanoma skin carcinomas occurred in 1.6% to 4.2% of patients, other types of malignancy in 0.7% to 2.1% of patients. Three-year safety data in renal and cardiac transplant patients did not reveal any unexpected changes in incidence of malignancy compared to the 1 year data.

    In pediatric patients, no other malignancies besides lymphoproliferative disorder (2/148 patients) have been observed.

    Severe neutropenia (ANC < 0.5 x 103/µL) developed in up to 2% of renal transplant patients, up to 2.8% of cardiac transplant patients and up to 3.6% of hepatic transplant patients receiving mycophenolate mofetil 3 g daily (see WARNINGS, Neutropenia; PRECAUTIONS,Laboratory Tests; andDOSAGE AND ADMINISTRATION).

    All transplant patients are at increased risk of opportunistic infections. The risk increases with total immunosuppressive load (see WARNINGS, Serious Infections and WARNINGS, New or Reactivated Viral Infections). Table 10 shows the incidence of opportunistic infections that occurred in the renal, cardiac, and hepatic transplant populations in the azathioprine-controlled prevention trials:

    Table 10: Viral and Fungal Infections in Controlled Studies in Prevention of Renal, Cardiac or Hepatic Transplant Rejection
      Renal Studies Cardiac Study Hepatic Study
    Mycophenolate Mofetil 2 g/day Mycophenolate Mofetil 3 g/day Azathioprine 1 to 2 mg/kg/day or 100 to 150 mg/day Mycophenolate Mofetil 3 g/day Azathioprine 1.5 to 3 mg/kg/day Mycophenolate Mofetil 3 g/day Azathioprine 1 to 2 mg/kg/day
    (n = 336) (n = 330) (n = 326) (n = 289) (n = 289) (n = 277) (n = 287)
    % % % % % % %
    Herpes simplex 16.7 20 19 20.8 14.5 10.1 5.9
    CMV              
    – Viremia/syndrome 13.4 12.4 13.8 12.1 10 14.1 12.2
    – Tissue invasive disease 8.3 11.5 6.1 11.4 8.7 5.8 8
    Herpes zoster 6 7.6 5.8 10.7 5.9 4.3 4.9
    – Cutaneous disease 6 7.3 5.5 10 5.5 4.3 4.9
    Candida 17 17.3 18.1 18.7 17.6 22.4 24.4
    – Mucocutaneous 15.5 16.4 15.3 18 17.3 18.4 17.4

    The following other opportunistic infections occurred with an incidence of less than 4% in mycophenolate mofetil patients in the above azathioprine-controlled studies: Herpes zoster, visceral disease; Candida, urinary tract infection, fungemia/disseminated disease, tissue invasive disease; Cryptococcosis; Aspergillus/Mucor; Pneumocystis carinii.

    In the placebo-controlled renal transplant study, the same pattern of opportunistic infection was observed compared to the azathioprine-controlled renal studies, with a notably lower incidence of the following: Herpes simplex and CMV tissue-invasive disease.

    In patients receiving mycophenolate mofetil (2 g or 3 g) in controlled studies for prevention of renal, cardiac or hepatic rejection, fatal infection/sepsis occurred in approximately 2% of renal and cardiac patients and in 5% of hepatic patients (see WARNINGS, Serious Infections).

    In cardiac transplant patients, the overall incidence of opportunistic infections was approximately 10% higher in patients treated with mycophenolate mofetil than in those receiving azathioprine, but this difference was not associated with excess mortality due to infection/sepsis among patients treated with mycophenolate mofetil.

    The following adverse events were reported with 3% to < 20% incidence in renal, cardiac, and hepatic transplant patients treated with mycophenolate mofetil, in combination with cyclosporine and corticosteroids.

    Table 11: Adverse Events Reported in 3% to < 20% of Patients Treated With Mycophenolate Mofetil in Combination With Cyclosporine and Corticosteroids
    Body System
    Body as a Whole abdomen enlarged, abscess, accidental injury, cellulitis, chills occurring with fever, cyst, face edema, flu syndrome, hemorrhage, hernia, lab test abnormal, malaise, neck pain, pelvic pain, peritonitis
    Hematologic and Lymphatic coagulation disorder, ecchymosis, pancytopenia, petechia, polycythemia, prothrombin time increased, thromboplastin time increased
    Urogenital acute kidney failure, albuminuria, dysuria, hydronephrosis, hematuria, impotence, kidney failure, kidney tubular necrosis, nocturia, oliguria, pain, prostatic disorder, pyelonephritis, scrotal edema, urine abnormality, urinary frequency, urinary incontinence, urinary retention, urinary tract disorder
    Cardiovascular angina pectoris, arrhythmia, arterial thrombosis, atrial fibrillation, atrial flutter, bradycardia, cardiovascular disorder, congestive heart failure, extrasystole, heart arrest, heart failure, hypotension, pallor, palpitation, pericardial effusion, peripheral vascular disorder, postural hypotension, pulmonary hypertension, supraventricular tachycardia, supraventricular extrasystoles, syncope, tachycardia, thrombosis, vasodilatation, vasospasm, ventricular extrasystole, ventricular tachycardia, venous pressure increased
    Metabolic and Nutritional abnormal healing, acidosis, alkaline phosphatase increased, alkalosis, bilirubinemia, creatinine increased, dehydration, gamma glutamyl transpeptidase increased, generalized edema, gout, hypercalcemia, hypercholesteremia, hyperlipemia, hyperphosphatemia, hyperuricemia, hypervolemia, hypocalcemia, hypochloremia, hypoglycemia, hyponatremia, hypophosphatemia, hypoproteinemia, hypovolemia, hypoxia, lactic dehydrogenase increased, respiratory acidosis, SGOT increased, SGPT increased, thirst, weight gain, weight loss
    Digestive anorexia, cholangitis, cholestatic jaundice, dysphagia, esophagitis, flatulence, gastritis, gastroenteritis, gastrointestinal disorder, gastrointestinal hemorrhage, gastrointestinal moniliasis, gingivitis, gum hyperplasia, hepatitis, ileus, infection, jaundice, liver damage, liver function tests abnormal, melena, mouth ulceration, nausea and vomiting, oral moniliasis, rectal disorder, stomach ulcer, stomatitis
    Respiratory apnea, asthma, atelectasis, bronchitis, epistaxis, hemoptysis, hiccup, hyperventilation, lung edema, lung disorder, neoplasm, pain, pharyngitis, pleural effusion, pneumonia, pneumothorax, respiratory disorder, respiratory moniliasis, rhinitis, sinusitis, sputum increased, voice alteration
    Skin and Appendages acne, alopecia, fungal dermatitis, hemorrhage, hirsutism, pruritus, rash, skin benign neoplasm, skin carcinoma, skin disorder, skin hypertrophy, skin ulcer, sweating, vesiculobullous rash
    Nervous agitation, anxiety, confusion, convulsion, delirium, depression, dry mouth, emotional lability, hallucinations, hypertonia, hypesthesia, nervousness, neuropathy, paresthesia, psychosis, somnolence, thinking abnormal, vertigo
    Endocrine Cushing’s syndrome, diabetes mellitus, hypothyroidism, parathyroid disorder
    Musculoskeletal arthralgia, joint disorder, leg cramps, myalgia, myasthenia, osteoporosis
    Special Senses abnormal vision, amblyopia, cataract (not specified), conjunctivitis, deafness, ear disorder, ear pain, eye hemorrhage, tinnitus, lacrimation disorder

    Pediatrics

    The type and frequency of adverse events in a clinical study in 100 pediatric patients 3 months to 18 years of age dosed with mycophenolate mofetil oral suspension 600 mg/m2 bid (up to 1 g bid) were generally similar to those observed in adult patients dosed with mycophenolate mofetil capsules at a dose of 1 g bid with the exception of abdominal pain, fever, infection, pain, sepsis, diarrhea, vomiting, pharyngitis, respiratory tract infection, hypertension, leukopenia, and anemia, which were observed in a higher proportion in pediatric patients.

    Mycophenolate Mofetil Intravenous

    The adverse event profile of mycophenolate mofetil intravenous was determined from a single, double-blind, controlled comparative study of the safety of 2 g/day of intravenous and oral mycophenolate mofetil in renal transplant patients in the immediate posttransplant period (administered for the first 5 days). The potential venous irritation of mycophenolate mofetil intravenous was evaluated by comparing the adverse events attributable to peripheral venous infusion of mycophenolate mofetil intravenous with those observed in the intravenous placebo group; patients in this group received active medication by the oral route.

    Adverse events attributable to peripheral venous infusion were phlebitis and thrombosis, both observed at 4% in patients treated with mycophenolate mofetil intravenous.

    In the active controlled study in hepatic transplant patients, 2 g/day of mycophenolate mofetil intravenous were administered in the immediate posttransplant period (up to 14 days). The safety profile of intravenous mycophenolate mofetil was similar to that of intravenous azathioprine.

    Postmarketing Experience

    Congenital Disorders: Embryofetal Toxicity: Congenital malformations and an increased incidence of first trimester pregnancy loss have been reported following exposure to mycophenolate mofetil during pregnancy (see PRECAUTIONS, Pregnancy).

    Digestive: Colitis (sometimes caused by cytomegalovirus), pancreatitis, isolated cases of intestinal villous atrophy.

    Hematologic and Lymphatic: Cases of pure red cell aplasia (PRCA) have been reported in patients treated with mycophenolate mofetil in combination with other immunosuppressive agents.

    Infections: (see WARNINGS, Serious Infections, New or Reactivated Viral Infections):

    • Serious life-threatening infections such as meningitis and infectious endocarditis have been reported occasionally.
    • There is evidence of a higher frequency of certain types of serious infections such as tuberculosis and atypical mycobacterial infection.
    • Cases of progressive multifocal leukoencephalopathy (PML), sometimes fatal, have been reported in patients treated with mycophenolate mofetil. The reported cases generally had risk factors for PML, including treatment with immunosuppressant therapies and impairment of immune function.
    • Polyomavirus associated neuropathy (PVAN), especially due to BK virus infection has been observed in patients receiving immunosuppressants, including mycophenolate mofetil. This infection is associated with serious outcomes, including deteriorating renal function and renal graft loss.
    • Viral reactivation has been reported in patients infected with HBV or HCV.

    Respiratory: Interstitial lung disorders, including fatal pulmonary fibrosis, have been reported rarely and should be considered in the differential diagnosis of pulmonary symptoms ranging from dyspnea to respiratory failure in posttransplant patients receiving mycophenolate mofetil.

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  • OVERDOSAGE

    The experience with overdose of mycophenolate mofetil in humans is very limited. The events received from reports of overdose fall within the known safety profile of the drug. The highest dose administered to renal transplant patients in clinical trials has been 4 g/day. In limited experience with cardiac and hepatic transplant patients in clinical trials, the highest doses used were 4 g/day or 5 g/day. At doses of 4 g/day or 5 g/day, there appears to be a higher rate, compared to the use of 3 g/day or less, of gastrointestinal intolerance (nausea, vomiting, and/or diarrhea), and occasional hematologic abnormalities, principally neutropenia, leading to a need to reduce or discontinue dosing.

    In acute oral toxicity studies, no deaths occurred in adult mice at doses up to 4000 mg/kg or in adult monkeys at doses up to 1000 mg/kg; these were the highest doses of mycophenolate mofetil tested in these species. These doses represent 11 times the recommended clinical dose in renal transplant patients and approximately 7 times the recommended clinical dose in cardiac transplant patients when corrected for BSA. In adult rats, deaths occurred after single-oral doses of 500 mg/kg of mycophenolate mofetil. The dose represents approximately 3 times the recommended clinical dose in cardiac transplant patients when corrected for BSA.

    MPA and MPAG are usually not removed by hemodialysis. However, at high MPAG plasma concentrations (> 100 mcg/mL), small amounts of MPAG are removed. By increasing excretion of the drug, MPA can be removed by bile acid sequestrants, such as cholestyramine (see CLINICAL PHARMACOLOGY, Pharmacokinetics).

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  • DOSAGE AND ADMINISTRATION

    Renal Transplantation

    Adults

    A dose of 1 g administered orally twice a day (daily dose of 2 g) is recommended for use in renal transplant patients. Although a dose of 1.5 g administered twice daily (daily dose of 3 g) was used in clinical trials and was shown to be safe and effective, no efficacy advantage could be established for renal transplant patients. Patients receiving 2 g/day of mycophenolate mofetil demonstrated an overall better safety profile than did patients receiving 3 g/day of mycophenolate mofetil.

    Pediatrics (3 Months to 18 Years of Age)

    The recommended dose of mycophenolate mofetil oral suspension is 600 mg/m2 administered twice daily (up to a maximum daily dose of 2 g/10 mL oral suspension). Patients with a body surface area of 1.25 m2 to 1.5 m2 may be dosed with mycophenolate mofetil capsules at a dose of 750 mg twice daily (1.5 g daily dose). Patients with a body surface area > 1.5 m2 may be dosed with mycophenolate mofetil capsules or tablets at a dose of 1 g twice daily (2 g daily dose).

    Cardiac Transplantation

    Adults

    A dose of 1.5 g bid oral (daily dose of 3 g) is recommended for use in adult cardiac transplant patients.

    Hepatic Transplantation

    Adults

    A dose of 1.5 g bid oral (daily dose of 3 g) is recommended for use in adult hepatic transplant patients.

    Mycophenolate Mofetil Capsules and Tablets

    The initial oral dose of mycophenolate mofetil capsules or mycophenolate mofetil tablets should be given as soon as possible following renal, cardiac or hepatic transplantation. Food had no effect on MPA AUC, but has been shown to decrease MPA Cmax by 40%. Therefore, it is recommended that mycophenolate mofetil capsules and mycophenolate mofetil tablets be administered on an empty stomach. However, in stable renal transplant patients, mycophenolate mofetil capsules and mycophenolate mofetil tablets may be administered with food if necessary.

    Patients should be instructed to take a missed dose as soon as they remember, except if it is near the next scheduled dose, and then continue to take mycophenolate mofetil at the usual times.

    Note: If required, mycophenolate mofetil oral suspension can be administered via a nasogastric tube with a minimum size of 8 French (minimum 1.7 mm interior diameter).  

    Patients With Hepatic Impairment

    No dose adjustments are recommended for renal patients with severe hepatic parenchymal disease. However, it is not known whether dose adjustments are needed for hepatic disease with other etiologies (see CLINICAL PHARMACOLOGY,Pharmacokinetics).

    No data are available for cardiac transplant patients with severe hepatic parenchymal disease.

    Geriatrics

    The recommended oral dose of 1 g bid for renal transplant patients, 1.5 g bid for cardiac transplant patients, and 1.5 g bid administered orally in hepatic transplant patients is appropriate for elderly patients (see PRECAUTIONS,Geriatric Use).

    Dosage Adjustments

    In renal transplant patients with severe chronic renal impairment (GFR < 25 mL/min/1.73 m2) outside the immediate posttransplant period, doses of mycophenolate mofetil capsules or mycophenolate mofetil tablets greater than 1 g administered twice a day should be avoided. These patients should also be carefully observed. No dose adjustments are needed in renal transplant patients experiencing delayed graft function postoperatively (see CLINICAL PHARMACOLOGY,Pharmacokineticsand PRECAUTIONS,Patients With Renal Impairment).

    No data are available for cardiac or hepatic transplant patients with severe chronic renal impairment. Mycophenolate mofetil capsules and mycophenolate mofetil tablets may be used for cardiac or hepatic transplant patients with severe chronic renal impairment if the potential benefits outweigh the potential risks.

    If neutropenia develops (ANC < 1.3 x 103/µL), dosing with mycophenolate mofetil capsules and mycophenolate mofetil tablets should be interrupted or the dose reduced, appropriate diagnostic tests performed, and the patient managed appropriately (see WARNINGS, Neutropenia;ADVERSE REACTIONS; and PRECAUTIONS,Laboratory Tests).

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  • HANDLING AND DISPOSAL

    Mycophenolate mofetil has demonstrated teratogenic effects in rats and rabbits (see Pregnancyand WARNINGS, Embryofetal Toxicity). Mycophenolate mofetil tablets should not be crushed and mycophenolate mofetil capsules should not be opened or crushed. Avoid inhalation or direct contact with skin or mucous membranes of the powder contained in mycophenolate mofetil capsules. If such contact occurs, wash thoroughly with soap and water; rinse eyes with plain water. Should a spill occur, wipe up using paper towels wetted with water to remove spilled powder.

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  • HOW SUPPLIED

    Mycophenolate Mofetil Capsules USP, 250 mg

    Mycophenolate mofetil capsules USP are available as follows:

    250 mg – hard gelatin capsules with a light blue opaque cap and a bright orange opaque body, filled with a white to off-white powder with small agglomerates; imprinted with "TEVA" on the cap and "7334" on the body. They are available in bottles of 100 and 500 capsules, and in unit-dose boxes of 100 capsules (10 x 10).

    Mycophenolate Mofetil Tablets USP, 500 mg

    Mycophenolate mofetil tablets USP are available as follows:

    500 mg – purple, oval-shaped, film-coated tablets, debossed with “93” on one side of the tablet and with “7477” on the other side. They are available in bottles of 100 and 500 tablets.

    Storage and Dispensing Information

    Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature].

    Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).

    KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

    All brand names listed are the registered trademarks of their respective owners and are not trademarks of Teva Pharmaceuticals USA.

     
    Manufactured In Israel By:

    TEVA PHARMACEUTICAL IND. LTD.

    Jerusalem, 91010, Israel

    Manufactured For:

    TEVA PHARMACEUTICALS USA

    Sellersville, PA 18960

    Rev. J 8/2013

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  • MEDICATION GUIDE

    Mycophenolate Mofetil Capsules USP, 250 mg

    Mycophenolate Mofetil Tablets USP, 500 mg

    Rx only

    Read the Medication Guide that comes with mycophenolate mofetil capsules and mycophenolate mofetil tablets before you start taking them and each time you refill your prescription. There may be new information. This Medication Guide does not take the place of talking with your doctor about your medical condition or your treatment.

    What is the most important information I should know about mycophenolate mofetil capsules and mycophenolate mofetil tablets?

    Mycophenolatemofetil capsules andmycophenolatemofetiltablets can cause serious side effects:

    • Increased risk of loss of a pregnancy (miscarriage) and higher risk of birth defects. Females who take mycophenolate mofetil during pregnancy have a higher risk of miscarriage during the first 3 months (first trimester), and a higher risk that their baby will be born with birth defects.

    If you are a female who can become pregnant:

    • your doctor must talk with you about acceptable birth control methods (contraceptive counseling) to use while taking mycophenolate mofetil.
    • you should have one pregnancy test immediately before starting mycophenolate mofetil and another pregnancy test 8 to 10 days later. Pregnancy tests should be repeated during routine follow-up visits with your doctor. Talk to your doctor about the results of all of your pregnancy tests.
    • you must use acceptable birth control during your entire mycophenolate mofetil therapy and for 6 weeks after stopping mycophenolate mofetil, unless at any time you choose to avoid sexual intercourse (abstinence) with a man completely.

    Mycophenolate mofetil decreases blood levels of the hormones in birth control pills that you take by mouth. Birth control pills may not work as well while you take mycophenolate mofetil, and you could become pregnant. If you take birth control pills while using mycophenolate mofetil you must also use another form of birth control. Talk to your doctor about other birth control methods that you can use while taking mycophenolate mofetil.

    If you plan to become pregnant, talk with your doctor. Your doctor will decide if other medicines to prevent rejection may be right for you.

    If you become pregnant while taking mycophenolate mofetil, do not stop taking mycophenolate mofetil. Call your doctor right away. In certain situations, you and your doctor may decide that taking mycophenolate mofetil is more important to your health than the possible risks to your unborn baby.

    • You and your doctor should report your pregnancy to
    • Mycophenolate Pregnancy Registry (1-800-617-8191)

    The purpose of this registry is to gather information about the health of you and your baby.

    • Increased risk of getting serious infections. Mycophenolate mofetil capsules and mycophenolate mofetil tablets weaken the body’s immune system and affect your ability to fight infections. Serious infections can happen with mycophenolate mofetil capsules and mycophenolate mofetil tablets and can lead to death. These serious infections can include:
      • Viral infections. Certain viruses can live in your body and cause active infections when your immune system is weak. Viral infections that can happen with mycophenolate mofetil capsules and mycophenolate mofetil tablets include:
        • Shingles, other herpes infections, and cytomegalovirus (CMV). CMV can cause serious tissue and blood infections.
        • BK virus. BK virus can affect how your kidney works and cause your transplanted kidney to fail.
        • Hepatitis B and C viruses. Hepatitis viruses can affect how your liver works. Talk to your doctor about how hepatitis viruses may affect you.
      • A brain infection called Progressive Multifocal Leukoencephalopathy (PML). In some patients, mycophenolate mofetil capsules and mycophenolate mofetil tablets may cause an infection of the brain that may cause death. You are at risk for this brain infection because you have a weakened immune system. You should tell your doctor right away if you have any of the following symptoms:
        • Weakness on one side of the body
        • You do not care about things that you usually care about (apathy)
        • You are confused or have problems thinking
        • You can not control your muscles
      • Fungal infections. Yeasts and other types of fungal infections can happen with mycophenolate mofetil capsules and mycophenolate mofetil tablets and can cause serious tissue and blood infections (see "What are the possible side effects of mycophenolate mofetil capsules and mycophenolate mofetil tablets?")

    Call your doctor right away if you have any of the following signs and symptoms of infection:

    • Temperature of 100.5°F or greater
    • Cold symptoms, such as a runny nose or sore throat
    • Flu symptoms, such as an upset stomach, stomach pain, vomiting or diarrhea
    • Earache or headache
    • Pain during urination
    • White patches in the mouth or throat
    • Unexpected bruising or bleeding
    • Cuts, scrapes or incisions that are red, warm and oozing pus
    • Increased risk of getting certain cancers. People who take mycophenolate mofetil capsules or mycophenolate mofetil tablets have a higher risk of getting lymphoma, and other cancers, especially skin cancer. Tell your doctor if you have:
      • unexplained fever, prolonged tiredness, weight loss or lymph node swelling
      • a brown or black skin lesion with uneven borders, or one part of the lesion does not look like the other
      • a change in the size and color of a mole
      • a new skin lesion or bump
      • any other changes to your health

    See the section “What are the possible side effects of mycophenolate mofetil capsules and mycophenolate mofetil tablets?” for information about other serious side effects.

    What are mycophenolate mofetil capsules and mycophenolate mofetil tablets?

    Mycophenolate mofetil capsules and mycophenolate mofetil tablets are a prescription medicine to prevent rejection (antirejection medicine) in people who have received a kidney, heart or liver transplant. Rejection is when the body’s immune system perceives the new organ as a “foreign” threat and attacks it.

    Mycophenolate mofetil capsules and mycophenolate mofetil tablets are used with other medicines called cyclosporines (Sandimmune®, Gengraf®, Neoral®) and corticosteroids.

    Mycophenolate mofetil capsules and mycophenolate mofetil tablets have been used safely and work in children who received a kidney transplant as they do in adults. It is not known if mycophenolate mofetil capsules and mycophenolate mofetil tablets are safe and work in children who receive a heart or liver transplant.

    Who should not take mycophenolate mofetil capsules or mycophenolate mofetil tablets?

    Do not take mycophenolate mofetil capsules or mycophenolate mofetil tablets if you are allergic to mycophenolate mofetil or any of the ingredients in mycophenolate mofetil capsules or mycophenolate mofetil tablets. See the end of this Medication Guide for a complete list of ingredients in mycophenolate mofetil capsules and mycophenolate mofetil tablets.

    What should I tell my doctor before taking mycophenolate mofetil capsules or mycophenolate mofetil tablets?

    Tell your doctor about all of your medical conditions, if you:

    • have any digestive problems, such as ulcers.
    • have Lesch-Nyhan or Kelley-Seegmiller syndrome or another rare inherited deficiency hypoxanthine-guanine phosphoribosyl-transferase (HGPRT). You should not take mycophenolate mofetil capsules or mycophenolate mofetil tablets if you have one of these disorders.
    • plan to receive any vaccines. People taking mycophenolate mofetil capsules or mycophenolate mofetil tablets should not take live vaccines. Some vaccines may not work as well during treatment with mycophenolate mofetil capsules or mycophenolate mofetil tablets.
    • are pregnant or are planning to become pregnant. See “What is the most important information I should know about mycophenolate mofetil capsules and mycophenolate mofetil tablets?
    • are breastfeeding or plan to breastfeed. It is not known if mycophenolate mofetil passes into breast milk. You and your doctor will decide if you will take mycophenolate mofetil capsules, mycophenolate mofetil tablets or breastfeed.

    Tell your healthcare provider about all of the medicines you are taking including prescription and nonprescription medicines, vitamins and herbal supplements. Some medicines may affect the way mycophenolate mofetil capsules and mycophenolate mofetil tablets work, and mycophenolate mofetil capsules and mycophenolate mofetil tablets may affect how some medicines work. Especially tell your doctor if you take:

    • birth control pills (oral contraceptives). See “What is the most important information I should know about mycophenolate mofetil capsules and mycophenolate mofetil tablets?
    • sevelamer (Renagel®, Renvela). These products should be taken 2 hours after taking mycophenolate mofetil capsules or mycophenolate mofetil tablets
    • acyclovir (Zovirax®), valacyclovir (Valtrex®), ganciclovir (Cytovene®-IV, Vitrasert®), valganciclovir (Valcyte®)
    • rifampin (Rifater®, Rifamate®, Rimactane®, Rifadin®)
    • antacids that contain magnesium and aluminum (mycophenolate mofetil capsules or mycophenolate mofetil tablets and the antacid should not be taken at the same time)
    • proton pump inhibitors (PPIs) (Prevacid®, Protonix®)
    • sulfamethoxazole/trimethoprim (Bactrim, Bactrim DS)
    • norfloxacin (Noroxin®) and metronidazole (Flagyl®, Flagyl® ER, Flagyl® IV, Metro IV, Helidac®, Pylera)
    • ciprofloxacin (Cipro®, Cipro® XR, Ciloxan®, Proquin® XR) and amoxicillin plus clavulanic acid (Augmentin®, Augmentin XR® )
    • azathioprine (Azasan®, Imuran®)
    • cholestyramine (Questran Light®, Questran®, Locholest Light, Locholest, Prevalite®)

    Know the medicines you take. Keep a list of them to show to your doctor or nurse and pharmacist when you get a new medicine. Do not take any new medicine without talking with your doctor.

    How should I take mycophenolate mofetil capsules and mycophenolate mofetil tablets?

    • Take mycophenolate mofetil capsules or mycophenolate mofetil tablets exactly as prescribed.
    • Do not stop taking mycophenolate mofetil capsules, mycophenolate mofetil tablets or change the dose unless your doctor tells you to.
    • If you miss a dose of mycophenolate mofetil capsules or mycophenolate mofetil tablets, or are not sure when you took your last dose, take the regular amount of mycophenolate mofetil capsules or mycophenolate mofetil tablets prescribed as soon as you remember. If it is time for your next dose, skip the missed dose and take your next dose at your normal scheduled time. Do not take 2 doses at the same time. Call your doctor if you are not sure what to do.
    • Take mycophenolate mofetil capsules and tablets on an empty stomach, either 1 hour before or 2 hours after a meal, unless your healthcare provider tells you otherwise. With the approval of your healthcare provider, in stable kidney transplant patients, mycophenolate mofetil capsules and mycophenolate mofetil tablets can be taken with food if necessary.
    • Most people take mycophenolate mofetil capsules or mycophenolate mofetil tablets by mouth either as light blue and bright orange capsules or purple tablets. Some people may get mycophenolate mofetil hydrochloride for injection soon after their transplant surgery as an infusion into a vein.
    • Do not crush mycophenolate mofetil tablets. Do not open or crush mycophenolate mofetil capsules.
    • If you are not able to swallow mycophenolate mofetil tablets or capsules, your doctor may prescribe mycophenolate mofetil oral suspension. This is a liquid form of mycophenolate mofetil. Your pharmacist will mix the medicine before giving it to you.
    • If you take too many mycophenolate mofetil capsules or mycophenolate mofetil tablets, call your doctor or the poison control center right away.

    What should I avoid while taking mycophenolate mofetil capsules and mycophenolate mofetil tablets?

    • Avoid pregnancy. See “What is the most important information I should know about mycophenolate mofetil capsules and mycophenolate mofetil tablets?
    • Limit the amount of time you spend in sunlight. Avoid using tanning beds or sunlamps. People who take mycophenolate mofetil capsules or mycophenolate mofetil tablets have a higher risk of getting skin cancer (see “What is the most important information I should know about mycophenolate mofetil capsules and mycophenolate mofetil tablets?”). Wear protective clothing when you are in the sun and use a sunscreen with a high protection factor (SPF 30 and above). This is especially important if your skin is very fair or if you have a family history of skin cancer.

    What are the possible side effects of mycophenolate mofetil capsules and mycophenolate mofetil tablets?

    Mycophenolate mofetil capsules and mycophenolate mofetil tablets can cause serious side effects:

    • See “What is the most important information I should know about mycophenolate mofetil capsules and mycophenolate mofetil tablets?
    • Low blood cell counts. People taking high doses of mycophenolate mofetil capsules or mycophenolate mofetil tablets each day may have a decrease in blood counts, including
      • white blood cells, especially neutrophils. Neutrophils fight against bacterial infections. You have a higher chance of getting an infection when your white blood cell count is low. This is most common from 3 months to 6 months after your transplant.
      • red blood cells. Red blood cells carry oxygen to your body tissues. You have a higher chance of getting severe anemia when your red blood cell count is low.
      • platelets. Platelets help with blood clotting.

    Your doctor will do blood tests before you start taking mycophenolate mofetil capsules or mycophenolate mofetil tablets and during treatment with mycophenolate mofetil capsules or mycophenolate mofetil tablets to check your blood cell counts.

    Tell your doctor right away if you have any signs of infection (see “What is the most important information I should knowaboutmycophenolate mofetil capsules and mycophenolate mofetil tablets?”), or any unexpected bruising or bleeding. Also, tell your doctor if you have unusual tiredness, lack of energy, dizziness or fainting.

    • Stomach problems. Stomach and intestinal bleeding can happen in people who take high doses of mycophenolate mofetil capsules or mycophenolate mofetil tablets. Bleeding can be severe and you may have to be hospitalized for treatment.

    Common side effects include:

    • diarrhea. Call your doctor right away if you have diarrhea. Do not stop taking mycophenolate mofetil capsules or mycophenolate mofetil tablets without first talking with your doctor.
    • vomiting
    • pain
    • stomach area pain
    • swelling of the lower legs, ankles and feet
    • high blood pressure

    Side effects that happen more often in children than in adults taking mycophenolate mofetil capsules or mycophenolate mofetil tablets include:

    • stomach area pain
    • fever
    • infection
    • pain
    • blood infection (sepsis)
    • diarrhea
    • vomiting
    • sore throat
    • colds (respiratory tract infections)
    • high blood pressure
    • low white blood cell count
    • low red blood cell count

    These are not all of the possible side effects of mycophenolate mofetil capsules and mycophenolate mofetil tablets. Tell your doctor about any side effect that bothers you or that does not go away.

    Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088 or to Teva USA, PHARMACOVIGILANCE at 1-866-832-8537.

    How should I store mycophenolate mofetil capsules and mycophenolate mofetil tablets?

    • Store mycophenolate mofetil capsules and mycophenolate mofetil tablets at room temperature, between 68°F to 77°F (20°C to 25°C). Keep the container closed tightly
    • Keep mycophenolate mofetil capsules, mycophenolate mofetil tablets and all medicines out of the reach of children

    General information about mycophenolate mofetil capsules and mycophenolate mofetil tablets

    Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use mycophenolate mofetil capsules or mycophenolate mofetil tablets for a condition for which they were not prescribed. Do not give mycophenolate mofetil capsules or mycophenolate mofetil tablets to other people, even if they have the same symptoms that you have. They may harm them.

    This Medication Guide summarizes the most important information about mycophenolate mofetil capsules and mycophenolate mofetil tablets. If you would like more information, talk with your doctor. You can ask your doctor or pharmacist for information about mycophenolate mofetil capsules and mycophenolate mofetil tablets that is written for healthcare professionals. For more information, call 1-888-838-2872.

    What are the ingredients in mycophenolate mofetil capsules USP and mycophenolate mofetil tablets USP?

    Active Ingredient: mycophenolate mofetil, USP

    Inactive Ingredients:

    Mycophenolate mofetil capsules, 250 mg: black iron oxide, croscarmellose sodium, D&C red #28, D&C yellow #10, FD&C blue #1, FD&C red #40, gelatin, magnesium stearate, povidone, pregelatinized starch, propylene glycol, shellac glaze, and titanium dioxide.

    Mycophenolate mofetil tablets, 500 mg: croscarmellose sodium, FD&C blue #2 aluminum lake, FD&C red #40 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, talc, and titanium dioxide.

    This Medication Guide has been approved by the U.S. Food and Drug Administration.

    For additional copies of this Medication Guide, please call 1-888-838-2872.

    All brand names listed are the registered trademarks of their respective owners and are not trademarks of Teva Pharmaceuticals USA.

     
    Manufactured In Israel By:

    TEVA PHARMACEUTICAL IND. LTD.

    Jerusalem, 91010, Israel

    Manufactured For:

    TEVA PHARMACEUTICALS USA

    Sellersville, PA 18960

    Rev. G 8/2013

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  • PRINCIPAL DISPLAY PANEL

    Mycophenolate Mofetil Capsules USP 250 mg 500s Label

    Mycophenolate Mofetil Capsules USP 250 mg 500s Label Text

    NDC 0093-7334-05

    MYCOPHENOLATE
    MOFETIL
    Capsules USP
    250 mg

    PHARMACIST: Dispense the accompanying
    Medication Guide to each patient.

    Rx only

    500 CAPSULES

    TEVA

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  • PRINCIPAL DISPLAY PANEL

    Mycophenolate Mofetil Tablets USP 500 mg 500s Label

    Mycophenolate Mofetil Tablets USP 500 mg 500s Label Text

    NDC 0093-7477-05

    MYCOPHENOLATE
    MOFETIL
    Tablets USP
    500 mg

    PHARMACIST: Dispense the accompanying
    Medication Guide to each patient.

    Rx only

    500 TABLETS

    TEVA

    Close
  • INGREDIENTS AND APPEARANCE
    MYCOPHENOLATE MOFETIL 
    mycophenolate mofetil capsule
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0093-7334
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MYCOPHENOLATE MOFETIL (MYCOPHENOLIC ACID) MYCOPHENOLATE MOFETIL 250 mg
    Inactive Ingredients
    Ingredient Name Strength
    FERROSOFERRIC OXIDE  
    CROSCARMELLOSE SODIUM  
    D&C RED NO. 28  
    D&C YELLOW NO. 10  
    FD&C BLUE NO. 1  
    FD&C RED NO. 40  
    GELATIN  
    MAGNESIUM STEARATE  
    POVIDONE K30  
    STARCH, CORN  
    PROPYLENE GLYCOL  
    SHELLAC  
    TITANIUM DIOXIDE  
    Product Characteristics
    Color BLUE (light blue) , ORANGE (bright orange) Score no score
    Shape CAPSULE Size 19mm
    Flavor Imprint Code TEVA;7334
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0093-7334-01 100 in 1 BOTTLE
    2 NDC:0093-7334-05 500 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA065491 05/06/2009
    MYCOPHENOLATE MOFETIL 
    mycophenolate mofetil tablet, film coated
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0093-7477
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MYCOPHENOLATE MOFETIL (MYCOPHENOLIC ACID) MYCOPHENOLATE MOFETIL 500 mg
    Inactive Ingredients
    Ingredient Name Strength
    CROSCARMELLOSE SODIUM  
    FD&C BLUE NO. 2  
    INDIGOTINDISULFONATE SODIUM  
    ALUMINUM OXIDE  
    FD&C RED NO. 40  
    HYPROMELLOSE 2910 (6 MPA.S)  
    MAGNESIUM STEARATE  
    CELLULOSE, MICROCRYSTALLINE  
    POLYETHYLENE GLYCOL 400  
    POVIDONE K30  
    TALC  
    TITANIUM DIOXIDE  
    Product Characteristics
    Color PURPLE Score no score
    Shape OVAL (oval-shaped) Size 18mm
    Flavor Imprint Code 93;7477
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0093-7477-01 100 in 1 BOTTLE
    2 NDC:0093-7477-05 500 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA065457 05/05/2009
    Labeler - Teva Pharmaceuticals USA Inc (118234421)
    Close