Label: READYSHARP DEXAMETHASONE- dexamethasone sodium phosphate injection

  • NDC Code(s): 53225-3660-1
  • Packager: Terrain Pharmaceuticals
  • Category: HUMAN PRESCRIPTION DRUG LABEL

Drug Label Information

Updated December 7, 2020

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  • DESCRIPTION

    Dexamethasone sodium phosphate, a synthetic adrenocortical steroid, is a white or slightly yellow crystalline powder. It is freely soluble in water and is exceedingly hygroscopic. The molecular weight is 516.41. It is designated chemically as 9-fluoro-11β,17-dihydroxy-16α-methyl-21-(phosphonooxy)pregna-1,4-diene-3, 20-dione disodium salt.

    The molecular formula is: C 22H 28FNa 2O 8P and the structural formula is:

    Structural formula

    Dexamethasone Sodium Phosphate Injection is a sterile solution of dexamethasone sodium phosphate for intravenous and intramuscular use. The 4 mg/mL strength may also be used for intra-articular, intralesional and soft tissue administration.

    Each mL of Dexamethasone Sodium Phosphate Injection 4 mg/mL contains dexamethasone sodium phosphate, equivalent to 4 mg dexamethasone phosphate or 3.33 mg dexamethasone. Inactive ingredients per mL: 1 mg sodium sulfite anhydrous, 19.4 mg sodium citrate anhydrous and 10.42 mg (0.01 mL) benzyl alcohol (preservative) in Water for Injection.

    Each mL of Dexamethasone Sodium Phosphate Injection 10 mg/mL contains dexamethasone sodium phosphate, equivalent to 10 mg dexamethasone phosphate or 8.33 mg dexamethasone. Inactive ingredients per mL: 1.5 mg sodium sulfite anhydrous, 16.5 mg sodium citrate anhydrous and 10.42 mg (0.01 mL) benzyl alcohol (preservative) in Water for Injection.

    The pH of both concentrations is 7.0-8.5; sodium hydroxide and/or citric acid used, if needed, for pH adjustment. Sealed under nitrogen.

  • CLINICAL PHARMACOLOGY

    Dexamethasone sodium phosphate injection has a rapid onset but short duration of action when compared with less soluble preparations. Because of this, it is suitable for the treatment of acute disorders responsive to adrenocortical steroid therapy.

    Naturally occurring glucocorticoids (hydrocortisone and cortisone), which also have salt-retaining properties, are used as replacement therapy in adrenocortical deficiency states. Their synthetic analogs, including dexamethasone, are primarily used for their potent anti-inflammatory effects in disorders of many organ systems.

    Glucocorticoids cause profound and varied metabolic effects. In addition, they modify the body's immune responses to diverse stimuli.

    At equipotent anti-inflammatory doses, dexamethasone almost completely lacks the sodium-retaining property of hydrocortisone and closely related derivatives of hydrocortisone.

  • INDICATIONS AND USAGE

    A. By Intravenous or Intramuscular Injection When Oral Therapy is not Feasible:

    1. ENDOCRINE DISORDERS

    Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance)

    Acute adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; mineralocorticoid supplementation may be necessary, particularly when synthetic analogs are used)

    Preoperatively, and in the event of serious trauma or illness, in patients with known adrenal insufficiency or when adrenocortical reserve is doubtful

    Shock unresponsive to conventional therapy if adrenocortical insufficiency exists or is suspected

    Congenital adrenal hyperplasia

    Nonsuppurative thyroiditis

    Hypercalcemia associated with cancer

    2. RHEUMATIC DISORDERS

    As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in:

    Post-traumatic osteoarthritis

    Synovitis of osteoarthritis

    Rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy)

    Acute and subacute bursitis

    Epicondylitis

    Acute nonspecific tenosynovitis

    Acute gouty arthritis

    Psoriatic arthritis

    Ankylosing spondylitis

    3. COLLAGEN DISEASES

    During an exacerbation or as maintenance therapy in selected cases of:

    Systemic lupus erythematosus

    Acute rheumatic carditis

    4. DERMATOLOGIC DISEASES

    Pemphigus

    Severe erythema multiforme (Stevens-Johnson syndrome)

    Exfoliative dermatitis

    Bullous dermatitis herpetiformis

    Severe seborrheic dermatitis

    Severe psoriasis

    Mycosis fungoides

    5. ALLERGIC STATES

    Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in:

    Bronchial asthma

    Contact dermatitis

    Atopic dermatitis

    Serum sickness

    Seasonal or perennial allergic rhinitis

    Drug hypersensitivity reactions

    Urticarial transfusion reactions

    Acute noninfectious laryngeal edema (epinephrine is the drug of first choice)

    6. OPHTHALMIC DISEASES

    Severe acute and chronic allergic and inflammatory processes involving the eye, such as:

    Herpes zoster ophthalmicus

    Iritis, iridocyclitis

    Chorioretinitis

    Diffuse posterior uveitis and choroiditis

    Optic neuritis

    Sympathetic ophthalmia

    Anterior segment inflammation

    Allergic conjunctivitis

    Keratitis

    Allergic corneal marginal ulcers

    7. GASTROINTESTINAL DISEASES

    To tide the patient over a critical period of the disease in:

    Ulcerative colitis (Systemic therapy)

    Regional enteritis (Systemic therapy)

    8. RESPIRATORY DISEASES

    Symptomatic sarcoidosis

    Berylliosis

    Fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy

    Loeffler's syndrome not manageable by other means

    Aspiration pneumonitis

    9. HEMATOLOGIC DISORDERS

    Acquired (autoimmune) hemolytic anemia

    Idiopathic thrombocytopenic purpura in adults (IV only; IM administration is contraindicated)

    Secondary thrombocytopenia in adults

    Erythroblastopenia (RBC anemia)

    Congenital (erythroid) hypoplastic anemia

    10. NEOPLASTIC DISEASES

    For palliative management of:

    Leukemias and lymphomas in adults

    Acute leukemia of childhood

    11. EDEMATOUS STATES

    To induce diuresis or remission of proteinuria in the nephrotic syndrome, without uremia, of the idiopathic type, or that due to lupus erythematosus

    12. MISCELLANEOUS

    Tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy

    Trichinosis with neurologic or myocardial involvement

    13. DIAGNOSTIC TESTING OF ADRENOCORTICAL HYPERFUNCTION

    14. CEREBRAL EDEMA associated with primary or metastatic brain tumor, craniotomy or head injury.  Use in cerebral edema is not a substitute for careful neurosurgical evaluation and definitive management such as neurosurgery or other specific therapy.

    B. By Intra-Articular or Soft Tissue Injection

    As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in:

    Synovitis of osteoarthritis

    Rheumatoid arthritis

    Acute and subacute bursitis

    Acute gouty arthritis

    Epicondylitis

    Acute nonspecific tenosynovitis

    Post-traumatic osteoarthritis

    C. By Intralesional Injection

    Keloids

    Localized hypertrophic, infiltrated, inflammatory lesions of: lichen planus, psoriatic plaques, granuloma annulare, and lichen simplex chronicus (neurodermatitis)

    Discoid lupus erythematosus

    Necrobiosis lipoidica diabeticorum

    Alopecia areata

    May also be useful in cystic tumors of an aponeurosis or tendon (ganglia).

  • CONTRAINDICATIONS

    Systemic fungal infections (see  WARNINGS regarding amphotericin B).

    Hypersensitivity to any component of this product, including sulfites (see WARNINGS).

  • WARNINGS

    Serious Neurologic Adverse Reactions with Epidural Administration

    Serious neurologic events, some resulting in death, have been reported with epidural injection of corticosteroids. Specific events reported include, but are not limited to, spinal cord infarction, paraplegia, quadriplegia, cortical blindness, and stroke. These serious neurologic events have been reported with and without use of fluoroscopy. The safety and effectiveness of epidural administration of corticosteroids has not been established, and corticosteroids are not approved for this use.

    General

    Because rare instances of anaphylactoid reactions have occurred in patients receiving parenteral corticosteroid therapy, appropriate precautionary measures should be taken prior to administration, especially when the patient has a history of allergy to any drug. Anaphylactoid and hypersensitivity reactions have been reported for Dexamethasone Sodium Phosphate Injection (see ADVERSE REACTIONS).

    Dexamethasone Sodium Phosphate Injection contains sodium sulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. The overall prevalence of sulfite sensitivity in the general population is unknown and probably low. Sulfite sensitivity is seen more frequently in asthmatic than in nonasthmatic people.

    Corticosteroids may exacerbate systemic fungal infections and, therefore, should not be used in the presence of such infections unless they are needed to control drug reactions due to amphotericin B. Moreover, there have been cases reported in which concomitant use of amphotericin B and hydrocortisone was followed by cardiac enlargement and congestive failure.

    In patients on corticosteroid therapy subjected to unusual stress, increased dosage of rapidly acting corticosteroids before, during and after the stressful situation is indicated.

    Drug-induced secondary adrenocortical insufficiency may result from too rapid withdrawal of corticosteroids and may be minimized by gradual reduction of dosage. This type of relative insufficiency may persist for months after discontinuation of therapy; therefore, in any situation of stress occurring during that period, hormone therapy should be reinstituted. If the patient is receiving steroids already, dosage may have to be increased. Since mineralocorticoid secretion may be impaired, salt and/or a mineralocorticoid should be administered concurrently.

    Corticosteroids may mask some signs of infection, and new infections may appear during their use. There may be decreased resistance and inability to localize infections when corticosteroids are used. Moreover, corticosteroids may affect the nitroblue-tetrazolium test for bacterial infection and produce false-negative results.

    In cerebral malaria, a double blind trial has shown that the use of corticosteroids is associated with prolongation of coma and a higher incidence of pneumonia and gastrointestinal bleeding.

    Corticosteroids may activate latent amebiasis. Therefore, it is recommended that latent or active amebiasis be ruled out before initiating corticosteroid therapy in any patient who has spent time in the tropics or in any patient with unexplained diarrhea.

    Prolonged use of corticosteroids may produce posterior subcapsular cataracts, glaucoma with possible damage to the optic nerves and may enhance the establishment of secondary ocular infections due to fungi or viruses.

    Average and large doses of cortisone or hydrocortisone can cause elevation of blood pressure, salt and water retention and increased excretion of potassium. These effects are less likely to occur with the synthetic derivatives except when used in large doses. Dietary salt restriction and potassium supplementation may be necessary. All corticosteroids increase calcium excretion.

    Administration of live virus vaccines, including smallpox, is contraindicated in individuals receiving immunosuppressive doses of corticosteroids. If inactivated viral or bacterial vaccines are administered to individuals receiving immunosuppressive doses of corticosteroids, the expected serum antibody response may not be obtained. However, immunization procedures may be undertaken in patients who are receiving corticosteroids as replacement therapy, e.g., for Addison's disease.

    Persons who are on drugs which suppress the immune system are more susceptible to infections than healthy individuals. Chickenpox and measles, for example, can have a more serious or even fatal course in non-immune children or adults on corticosteroids. In such children or adults who have not had these diseases, particular care should be taken to avoid exposure. How the dose, route and duration of corticosteroid administration affects the risk of developing a disseminated infection is unknown. The contribution of the underlying disease and/or prior corticosteroid treatment to the risk is also not known. If exposed to chickenpox, prophylaxis with varicella zoster immune globulin (VZIG) may be indicated. If exposed to measles, prophylaxis with pool intramuscular immune globulin (IG) may be indicated. (See the respective package inserts for VZIG and IG for complete prescribing information.) If chickenpox develops, treatment with antiviral agents may be considered.

    The use of Dexamethasone Sodium Phosphate Injection in active tuberculosis should be restricted to those cases of fulminating or disseminated tuberculosis in which the corticosteroid is used for the management of the disease in conjunction with an appropriate antituberculosis regimen.

    If corticosteroids are indicated in patients with latent tuberculosis or tuberculin reactivity, close observation is necessary as reactivation of the disease may occur. During prolonged corticosteroid therapy, these patients should receive chemoprophylaxis.

    Literature reports suggest an apparent association between use of corticosteroids and left ventricular free wall rupture after a recent myocardial infarction; therefore, therapy with corticosteroids should be used with great caution in these patients.

    Usage in Pregnancy

    Since adequate human reproduction studies have not been done with corticosteroids, use of these drugs in pregnancy or in women of childbearing potential requires that the anticipated benefits be weighed against the possible hazards to the mother and embryo or fetus. Infants born of mothers who have received substantial doses of corticosteroids during pregnancy should be carefully observed for signs of hypoadrenalism.

    Corticosteroids appear in breast milk and could suppress growth, interfere with endogenous corticosteroid production or cause other unwanted effects. Mothers taking pharmacologic doses of corticosteroids should be advised not to nurse.

  • PRECAUTIONS

    General

    This product, like many other steroid formulations, is sensitive to heat. Therefore, it should not be autoclaved when it is desirable to sterilize the exterior of the vial.

    Following prolonged therapy, withdrawal of corticosteroids may result in symptoms of the corticosteroid withdrawal syndrome including fever, myalgia, arthralgia and malaise. This may occur in patients even without evidence of adrenal insufficiency.

    There is an enhanced effect of corticosteroids in patients with hypothyroidism and in those with cirrhosis.

    Corticosteroids should be used cautiously in patients with ocular herpes simplex for fear of corneal perforation.

    The lowest possible dose of corticosteroid should be used to control the condition under treatment, and when reduction in dosage is possible, the reduction must be gradual.

    Psychic derangements may appear when corticosteroids are used, ranging from euphoria, insomnia, mood swings, personality changes and severe depression to frank psychotic manifestations. Also, existing emotional instability or psychotic tendencies may be aggravated by corticosteroids.

    Aspirin should be used cautiously in conjunction with corticosteroids in hypoprothrombinemia.

    Steroids should be used with caution in nonspecific ulcerative colitis, if there is a probability of impending perforation, abscess, or other pyogenic infection, also in diverticulitis, fresh intestinal anastomoses, active or latent peptic ulcer, renal insufficiency, hypertension, osteoporosis and myasthenia gravis. Signs of peritoneal irritation following gastrointestinal perforation in patients receiving large doses of corticosteroids may be minimal or absent. Fat embolism has been reported as a possible complication of hypercortisonism.

    When large doses are given, some authorities advise that antacids be administered between meals to help prevent peptic ulcer.

    Growth and development of infants and children on prolonged corticosteroid therapy should be carefully followed.

    Steroids may increase or decrease motility and number of spermatozoa in some patients.

    Phenytoin, phenobarbital, ephedrine and rifampin may enhance the metabolic clearance of corticosteroids resulting in decreased blood levels and lessened physiologic activity, thus requiring adjustment in corticosteroid dosage. These interactions may interfere with dexamethasone suppression tests which should be interpreted with caution during administration of these drugs.

    False negative results in the dexamethasone suppression test (DST) in patients being treated with indomethacin have been reported. Thus, results of the DST should be interpreted with caution in these patients.

    The prothrombin time should be checked frequently in patients who are receiving corticosteroids and coumarin anticoagulants at the same time because of reports that corticosteroids have altered the response to these anticoagulants. Studies have shown that the usual effect produced by adding corticosteroids is inhibition of response to coumarins, although there have been some conflicting reports of potentiation not substantiated by studies.

    When corticosteroids are administered concomitantly with potassium-depleting diuretics, patients should be observed closely for development of hypokalemia.

    Intra-articular injection of a corticosteroid may produce systemic as well as local effects.

    Appropriate examination of any joint fluid present is necessary to exclude a septic process.

    A marked increase in pain accompanied by local swelling, further restriction of joint motion, fever and malaise is suggestive of septic arthritis. If this complication occurs and the diagnosis of sepsis is confirmed, appropriate antimicrobial therapy should be instituted.

    Injection of a steroid into an infected site is to be avoided.

    Corticosteroids should not be injected into unstable joints.

    Patients should be impressed strongly with the importance of not overusing joints in which symptomatic benefit has been obtained as long as the inflammatory process remains active.

    Frequent intra-articular injection may result in damage to joint tissues.

    The slower rate of absorption by intramuscular administration should be recognized.

    Information for Patients

    Persons who are on immunosuppressant doses of corticosteroids should be warned to avoid exposure to chickenpox or measles. Patients should also be advised that if they are exposed, medical advice should be sought without delay.

  • ADVERSE REACTIONS

    Fluid and Electrolyte Disturbances

    Sodium retention

    Fluid retention

    Congestive heart failure in susceptible patients

    Potassium loss

    Hypokalemic alkalosis

    Hypertension

    Musculoskeletal

    Muscle weakness

    Steroid myopathy

    Loss of muscle mass

    Osteoporosis

    Vertebral compression fractures

    Aseptic necrosis of femoral and humeral heads

    Pathologic fracture of long bones

    Tendon rupture

    Gastrointestinal

    Peptic ulcer with possible subsequent perforation and hemorrhage

    Perforation of the small and large bowel, particularly in patients with inflammatory bowel disease

    Pancreatitis

    Abdominal distention

    Ulcerative esophagitis

    Dermatologic

    Impaired wound healing

    Thin, fragile skin

    Petechiae and ecchymoses

    Erythema

    Increased sweating

    May suppress reactions to skin tests

    Burning or tingling, especially in the perineal area (after IV injection)

    Other cutaneous reactions, such as allergic dermatitis, urticaria, angioneurotic edema

    Neurologic

    Convulsions

    Increased intracranial pressure with papilledema (pseudotumor cerebri) usually after treatment

    Vertigo

    Headache

    Psychic disturbances

    Endocrine

    Menstrual irregularities

    Development of cushingoid state

    Suppression of growth in children

    Secondary adrenocortical and pituitary unresponsiveness, particularly in times of stress, as in trauma, surgery or illness

    Decreased carbohydrate tolerance

    Manifestations of latent diabetes mellitus

    Increased requirements for insulin or oral hypoglycemic agents in diabetics

    Hirsutism

    Ophthalmic

    Posterior subcapsular cataracts

    Increased intraocular pressure

    Glaucoma

    Exophthalmos

    Metabolic

    Negative nitrogen balance due to protein catabolism

    Cardiovascular

    Myocardial rupture following recent myocardial infarction (see WARNINGS)

    Other

    Anaphylactoid or hypersensitivity reactions

    Thromboembolism

    Weight gain

    Increased appetite

    Nausea

    Malaise

    Hiccups

    The following additional adverse reactions are related to parenteral corticosteroid therapy:

    Rare instances of blindness associated with intralesional therapy around the face and head

    Hyperpigmentation or hypopigmentation

    Subcutaneous and cutaneous atrophy

    Sterile abscess

    Postinjection flare (following intra-articular use)

    Charcot-like arthropathy

  • OVERDOSAGE

    Reports of acute toxicity and/or death following overdosage of glucocorticoids are rare. In the event of overdosage, no specific antidote is available; treatment is supportive and symptomatic.

    The oral LD 50 of dexamethasone in female mice was 6.5 g/kg. The intravenous LD 50 of dexamethasone sodium phosphate in female mice was 794 mg/kg.

  • DOSAGE AND ADMINISTRATION

    Dexamethasone Sodium Phosphate Injection, 4 mg/mL- For intravenous, intramuscular, intra-articular, intralesional and soft tissue injection.

    Dexamethasone Sodium Phosphate Injection, 10 mg/mL- For intravenous and intramuscular injection only.

    Dexamethasone Sodium Phosphate Injection can be given directly from the vial or it can be added to Sodium Chloride Injection or Dextrose Injection and administered by intravenous drip.

    Solutions used for intravenous administration or further dilution of this product should be preservative-free when used in the neonate, especially the premature infant.

    When it is mixed with an infusion solution, sterile precautions should be observed. Since infusion solutions generally do not contain preservatives, mixtures should be used within 24 hours.

    DOSAGE REQUIREMENTS ARE VARIABLE AND MUST BE INDIVIDUALIZED ON THE BASIS OF THE DISEASE AND THE RESPONSE OF THE PATIENT.

    Intravenous and Intramuscular Injection

    The initial dosage of Dexamethasone Sodium Phosphate Injection varies from 0.5 to 9 mg a day depending on the disease being treated. In less severe diseases doses lower than 0.5 mg may suffice, while in severe diseases doses higher than 9 mg may be required.

    The initial dosage should be maintained or adjusted until the patient's response is satisfactory. If a satisfactory clinical response does not occur after a reasonable period of time, discontinue Dexamethasone Sodium Phosphate Injection and transfer the patient to other therapy.

    After a favorable initial response, the proper maintenance dosage should be determined by decreasing the initial dosage in small amounts to the lowest dosage that maintains an adequate clinical response.

    Patients should be observed closely for signs that might require dosage adjustment, including changes in clinical status resulting from remissions or exacerbations of the disease, individual drug responsiveness and the effect of stress (e.g., surgery, infection, trauma). During stress it may be necessary to increase dosage temporarily.

    If the drug is to be stopped after more than a few days of treatment, it usually should be withdrawn gradually.

    When the intravenous route of administration is used, dosage usually should be the same as the oral dosage. In certain overwhelming, acute, life-threatening situations, however, administration in dosages exceeding the usual dosages may be justified and may be in multiples of the oral dosages. The slower rate of absorption by intramuscular administration should be recognized.

    SHOCK

    There is a tendency in current medical practice to use high (pharmacologic) doses of corticosteroids for the treatment of unresponsive shock. The following dosages of Dexamethasone Sodium Phosphate Injection have been suggested by various authors:

      Author*  Dosage
     Cavanagh 1

      3 mg/kg of body weight per 24 hours by constant intravenous infusion after an initial intravenous injection of 20 mg

     Dietzman 2

      2 to 6 mg/kg of body weight as a single intravenous injection

     Frank 3

      40 mg initially followed by repeat intravenous injection every 4 to 6 hours while shock persists

     Oaks 4

      40 mg initially followed by repeat intravenous injection every 2 to 6 hours while shock persists

     Schumer 5

      1 mg/kg of body weight as a single intravenous injection

    Administration of high dose corticosteroid therapy should be continued only until the patient's condition has stabilized and usually not longer than 48 to 72 hours.

    Although adverse reactions associated with high dose, short term corticosteroid therapy are uncommon, peptic ulceration may occur.

    CEREBRAL EDEMA

    Dexamethasone Sodium Phosphate Injection is generally administered initially in a dosage of 10 mg intravenously followed by four mg every six hours intramuscularly until the symptoms of cerebral edema subside. Response is usually noted within 12 to 24 hours and dosage may be reduced after two to four days and gradually discontinued over a period of five to seven days. For palliative management of patients with recurrent or inoperable brain tumors, maintenance therapy with two mg two or three times a day may be effective.

    ACUTE ALLERGIC DISORDERS

    In acute, self-limited allergic disorders or acute exacerbations of chronic allergic disorders the following dosage schedule combining parenteral and oral therapy is suggested:

    Dexamethasone Sodium Phosphate Injection, 4 mg/mL - First day, 1 or 2 mL (4 or 8 mg) intramuscularly.

    Dexamethasone tablets, 0.75 mg - Second and third days, 4 tablets in two divided doses each day; fourth day 2 tablets in two divided doses; fifth and sixth days, 1 tablet each day; seventh day, no treatment; eighth day, follow-up visit.

    This schedule is designed to ensure adequate therapy during acute episodes, while minimizing the risk of overdosage in chronic cases.

    Intra-articular, Intralesional and Soft Tissue Injection

    Intra-articular, intralesional and soft tissue injections are generally employed when the affected joints or areas are limited to one or two sites. Dosage and frequency of injection varies depending on the condition and the site of injection. The usual dose is from 0.2 to 6 mg. The frequency usually ranges from once every three to five days to once every two to three weeks. Frequent intra-articular injection may result in damage to joint tissues. Some of the usual single doses are:

    Site of InjectionAmount of Dexamethasone Phosphate (mg)
    Large Joints (e.g., knee)2 to 4
    Small Joints (e.g., Interphalangeal, Temporomandibular)0.8 to 1
    Bursae2 to 3
    Tendon Sheaths0.4 to 1
    Soft Tissue Infiltration2 to 6
    Ganglia1 to 2

    Dexamethasone Sodium Phosphate Injection is particularly recommended for use in conjunction with one of the less soluble, longer-acting steroids for intra-articular and soft tissue injection.

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever the solution and container permit.

  • HOW SUPPLIED

    Dexamethasone Sodium Phosphate Injection, USP is available in the following packages:

    4 mg/mL
      1 mL vials packaged in 25s (NDC 0641-6145-25)
      5 mL vials packaged in 25s (NDC 0641-6146-25)

    10 mg/mL
      1 mL vials packaged in 25s (NDC 0641-0367-25)

    Storage

    Protect from light: Keep covered in carton until time of use. Store at 20°-25°C (68°-77°F), excursions permitted to 15°-30°C (59°-86°F) [See USP Controlled Room Temperature]. Avoid freezing. Do not use if solution is hazy or has a precipitate. Do not autoclave.

    To report SUSPECTED ADVERSE REACTIONS, contact West-Ward Pharmaceuticals Corp. at 1-877-845-0689, or the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    For Product Inquiry call 1-877-845-0689.

  • REFERENCES

    *1. Cavanagh, D.; Singh, K. B.: Endotoxin shock in pregnancy and abortion, in: "Corticosteroids in the Treatment of Shock", Schumer, W.; Nyhus, L. M., Editors, Urbana, University of Illinois Press, 1970, pp. 86-96.

    2. Dietzman, R. H.; Ersek, R. A.; Bloch, J. M.; Lillehei, R. C.: High-output, low-resistance, gram-negative septic shock in man, Angiology 20: 691-700, Dec. 1969.

    3. Frank, E.: Clinical observations in shock and management (In: Shields, T. F., ed.: Symposium on current concepts and management of shock), J. Maine Med. Ass. 59: 195-200, Oct. 1968.

    4. Oaks, W. W.; Cohen, H. E.: Endotoxin shock in the geriatric patient, Geriat. 22: 120-130, Mar. 1967.

    5. Schumer, W.; Nyhus, L. M.: Corticosteroid effect on biochemical parameters of human oligemic shock, Arch. Surg. 100: 405-408, Apr. 1970.

    Manufactured by:

    WEST-WARD
    A HIKMA COMPANY
    Eatontown, NJ 07724 USA

    Revised June 2016

    462-331-04

  • Principal Display Panel - Vial

    vial

    NDC 0641-0367-21

    Dexamethasone
    Sodium Phosphate
    Injection, USP
    10 mg/mL Rx only

    (dexamethasone phosphate equivalent)
    1 mL Vial
    FOR IV OR IM USE ONLY
    PROTECT FROM LIGHT

  • Principal Display Panel

    dex

    ReadySharp Dexamethasone

    CONTENTS:

    1 Dexamethasone Sodium Phosphate 10 mg, 1 mL
    1 Sterile Alcohol Prep Pad

    1 Adhesive Bandage

    3 Povidone-Iodine Swabsticks

    1 Retractable Syringe w/ Needle 23G x 1

    NDC 53225-3660-1

    REF TRNRSS3660

    Packaged in the USA for:

    Terrain Pharmaceuticals

    Reno, NV 89501

    877-985-8377

    ReadySharp.us

    Non-Sterile

    Single Use Only

    RI16DYN 16-513

    CAUTION: Federal law restricts this device for sale by or on the order of a physician. This package has not been terminally sterilized. Individual items in package can be sterile where indicated by the original manufacturer. Do not sterilize. Store between 59°F – 86°F.

  • INGREDIENTS AND APPEARANCE
    READYSHARP DEXAMETHASONE 
    dexamethasone sodium phosphate injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:53225-3660
    Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXAMETHASONE SODIUM PHOSPHATE (UNII: AI9376Y64P) (DEXAMETHASONE - UNII:7S5I7G3JQL) DEXAMETHASONE PHOSPHATE10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM SULFITE (UNII: VTK01UQK3G) 1.5 mg  in 1 mL
    SODIUM CITRATE (UNII: 1Q73Q2JULR) 16.5 mg  in 1 mL
    BENZYL ALCOHOL (UNII: LKG8494WBH) 10.42 mg  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53225-3660-11 mL in 1 VIAL; Type 0: Not a Combination Product10/26/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA08770209/07/1982
    Labeler - Terrain Pharmaceuticals (078358750)