FEIBA NF- anti-inhibitor coagulant complex
Baxalta Incorporated
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FEIBA NF (Anti-Inhibitor Coagulant Complex)
DESCRIPTION
FEIBA NF (Anti-Inhibitor Coagulant Complex), nanofiltered and vapor heated, is a freeze-dried sterile human plasma fraction with Factor VIII inhibitor bypassing activity. In vitro, FEIBA NF shortens the activated partial thromboplastin time (APTT) of plasma containing Factor VIII inhibitor. Factor VIII inhibitor bypassing activity is expressed in arbitrary units. One unit of activity is defined as that amount of FEIBA NF that shortens the APTT of a high titer Factor VIII inhibitor reference plasma to 50% of the blank value.
FEIBA NF contains Factors II, IX, and X, mainly non-activated, and Factor VII mainly in the activated form. The product contains approximately equal unitages of Factor VIII inhibitor bypassing activity and Prothrombin Complex Factors. In addition, 1–6 units of Factor VIII coagulant antigen (FVIII C:Ag) per mL are present. The preparation contains only traces of factors of the kinin generating system. It contains no heparin.
Reconstituted FEIBA NF contains 4 mg of trisodium citrate and 8 mg of sodium chloride per mL.
FEIBA NF is manufactured from large plasma pools of human plasma. Screening against potentially infectious agents begins with the donor selection process and continues throughout plasma collection and plasma preparation. Each individual plasma donation used in the manufacture of FEIBA NF is collected only at FDA approved blood establishments and is tested by FDA licensed serological tests for Hepatitis B Surface Antigen (HBsAg), and for antibodies to Human Immunodeficiency Virus (HIV-1/HIV-2) and Hepatitis C Virus (HCV) in accordance with the U.S. regulatory requirements. As an additional safety measure, mini-pools of the plasma are tested for the presence of HIV-1 and HCV by FDA licensed Nucleic Acid Testing (NAT) and found negative. In addition, two dedicated and independent virus removal/inactivation steps have been integrated into the manufacturing process, namely 35 nm nanofiltration and a vapor heat treatment process. In addition, the DEAE-Sephadex adsorption contributes to the virus safety profile of FEIBA NF. Despite these measures, such products can still potentially transmit disease (see WARNINGS).
In vitro spiking studies have been used to validate the capability of the manufacturing process to remove and inactivate viruses. To establish the minimum applicable virus clearance capacity of the manufacturing process, these virus clearance studies were performed under extreme conditions (e.g. at minimum incubation times and temperatures below specifications for vapor-heat treatment). Virus clearance studies for FEIBA NF performed in accordance with good laboratory practices have demonstrated, that the manufacturing process of FEIBA NF ensures a high margin of safety with respect to adventitious viruses (Table 1).
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| Virus Type | Enveloped RNA | Enveloped DNA | Non-enveloped RNA | Non-enveloped DNA | |||
|
Virus Family |
Retroviridae |
Flaviviridae |
Herpesviridae |
Picornaviridae |
Parvoviridae |
||
| Virus* | HIV-1 | BVDV | WNV | PRV | HAV | B19V† | MMV |
| DEAE Sephadex Adsorption | 3.2 | 1.8 | n.d. | 2.5 | 1.5 | 1.7 | 1.2 |
| 35 nm Nanofiltration | > 5.3 | 2.1 | 4.7 | > 5.7 | 2.6 | 0.2‡ | 1.0 |
| Vapor-Heat Treatment | > 5.9 | > 5.6 | > 8.1 | > 6.7 | > 5.2 | 3.5 | 0.9‡ |
| Overall log reduction factor (ORF) | > 14.4 | > 9.5 | > 12.8 | > 14.9 | > 9.3 | 5.2 | 2.2 |
CLINICAL STUDIES
FEIBA NF is identical in formulation to FEIBA VH. Biochemical and preclinical studies have confirmed the comparability of FEIBA NF and FEIBA VH.
The safety and efficacy of FEIBA has been demonstrated by two prospective clinical trials1,2. The first, conducted by Sixma and collaborators, was a randomized double-blind study comparing the effect of FEIBA and PROTHROMPLEX IMMUNO (a non-activated prothrombin complex concentrate) in 15 patients with hemophilia A and inhibitors to Factor VIII. A total of 150 bleeding episodes (primarily joint and musculoskeletal plus a few mucocutaneous) were treated. A single dose of 88 Units per kg of body weight was used uniformly for treatments with FEIBA . The study showed that, based on subjective patient evaluation, FEIBA was fully effective in 41.0% and partly effective in 24.6% of episodes (i.e. combined effectiveness of 65.6%), while PROTHROMPLEX IMMUNO was rated fully effective in 25.0% and partly effective in 21.4% of episodes (i.e. combined effectiveness of 46.4%).
The second study with FEIBA was a multicenter study conducted by Hilgartner et al2. This study was conducted in 44 hemophilia A subjects with inhibitors, 3 hemophilia B subjects with inhibitors and 2 acquired FVIII inhibitor subjects. It was designed to evaluate the efficacy of FEIBA in the treatment of joint, mucous membrane, musculocutaneous and emergency bleeding episodes such as central nervous system hemorrhages and surgical bleedings. In 49 patients with inhibitor titers of greater than 5 Bethesda Units (from nine co-operating hemophilia centers), 489 single doses were given for the treatment of 165 bleeding episodes. The usual dosage was 50 Units per kg of body weight, repeated at 12-hour intervals (6-hour intervals in mucous membrane bleedings), if necessary. Bleeding was controlled in 153 episodes (93%). In 130 (78%) of the episodes, hemostasis was achieved with one or more infusions within 36 hours. Of these, 36% were controlled with one infusion within 12 hours. An additional 14% of episodes responded after more than 36 hours.
Of the 489 single doses, 18 (3.7%) caused minor transient reactions in recipients. Out of 49 patients, 10 (20%) showed a rise in their inhibitor titers. In 5 of these patients (10%), the rise was tenfold or more. However, of these 10 patients, 3 had received Factor VIII or Factor IX concentrates within 2 weeks prior to treatment with FEIBA. These anamnestic rises have not been observed to interfere with the efficacy of FEIBA.
INDICATIONS AND USAGE
FEIBA NF (Anti-Inhibitor Coagulant Complex) is indicated for the control of spontaneous bleeding episodes or to cover surgical interventions in hemophilia A and hemophilia B patients with inhibitors.
Clinical experience suggests that patients with a Factor VIII inhibitor titer of less than 5 B.U. may be successfully treated with Antihemophilic Factor. Patients with titers ranging between 5 and 10 B.U. may either be treated with Antihemophilic Factor or FEIBA NF. Cases with Factor VIII inhibitor titers greater than 10 B.U. have generally been refractory to treatment with Antihemophilic Factor.
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| Patient's Inhibitor | Clinical Situation | ||
| Titer | Minor Bleeding | Major Bleeding | Surgery (Emergency) |
| less than 5 B.U. | AHF* | AHF | AHF |
| 5 to 10 B.U. | AHF | AHF | AHF |
| FEIBA NF | FEIBA NF | FEIBA NF | |
| more than 10 B.U. | FEIBA NF | FEIBA NF | FEIBA NF |
Inadequate response to treatment may result from an abnormal platelet count or impaired platelet function3-5 that were present before treatment with FEIBA NF, nanofiltered and vapor-heated.
CONTRAINDICATIONS
The use of FEIBA NF is contraindicated:
- in patients who have known anaphylactic or severe hypersensitivity reactions to the product.
- in patients who are known to have a normal coagulation mechanism.
- for the treatment of bleeding episodes resulting from coagulation factor deficiencies in the absence of inhibitors to coagulation factor VIII or coagulation factor IX.
- in patients with significant signs of disseminated intravascular coagulation (DIC).
- in patients with acute thrombosis or embolism (including myocardial infarction).
WARNINGS
At first sign or symptom of an infusion/hypersensitivity reaction or a thrombotic/thromboembolic event, FEIBA NF administration should be stopped immediately and diagnostic and therapeutic measures initiated as appropriate.
Anaphylaxis and Hypersensitivity Reactions
Allergic-type hypersensitivity reactions, including severe anaphylactoid reactions, have been reported following the infusion of FEIBA. The symptoms include urticaria, angioedema, gastrointestinal manifestations, bronchospasm, and hypotension; these reactions can be severe and can be systemic (e.g., anaphylaxis with urticaria and angioedema, bronchospasm, and circulatory shock). If signs and symptoms of severe allergic reactions occur, immediately discontinue administration of FEIBA NF and provide appropriate supportive care. Have epinephrine immediately available to treat, if appropriate, any acute severe hypersensitivity reactions. Other infusion reactions, such as chills, pyrexia, and hypertension have also been reported.
In patients with known or suspected hypersensitivity to FEIBA NF, the expected benefit and the risk of re-exposure must be carefully weighed, taking into account the known or suspected type of the patient's hypersensitivity (allergic or non-allergic), including potential remedial and/or preventative therapy or alternative therapeutic agents.
Thrombotic and Thromboembolic Events
Thrombotic and thromboembolic events [including disseminated intravascular coagulation (DIC), venous thrombosis, pulmonary embolism, myocardial infarction, and stroke] have been reported following infusion of FEIBA VH or FEIBA NF, particularly following the administration of high doses and/or in patients with thrombotic risk factors (see ADVERSE REACTIONS). The possible presence of such risk factors should always be considered in patients with congenital and acquired hemophilia. Thromboembolic events are well recognized potential complications of FEIBA infusion. Many of these events occurred with doses above 200 units/kg/day or in patients with other risk factors for thromboembolic events. A single dose of 100 units/kg body weight and a daily dose of 200 units/kg body weight should not be exceeded unless the severity of bleeding warrants and justifies the use of higher doses. Patients receiving more than 100 units/kg of body weight of FEIBA NF must be monitored for the development of DIC and/or symptoms of acute coronary ischemia. High doses of FEIBA NF should be given only as long as absolutely necessary to stop bleeding.
Patients with disseminated intravascular coagulation (DIC), advanced atherosclerotic disease, crush injury, septicemia, or concomitant treatment with recombinant factor VIIa have an increased risk of developing thrombotic events due to circulating tissue factor (TF) or predisposing coagulopathy.
FEIBA VH or FEIBA NF should be used with particular caution and only if there are no therapeutic alternatives in patients at risk of DIC, arterial or venous thrombosis.
FEIBA NF should not be given to patients with significant signs of disseminated intravascular coagulation (DIC) or fibrinolysis. Infusion of FEIBA NF should not exceed single dosage of 100 units per kg of body weight and daily doses of 200 units per kg body weight. Thrombotic events have been identified through post-marketing surveillance following FEIBA use for each of the approved indications. The incidence of thrombotic events cannot be determined from post-marketing data.
Transmission of Infectious Agents
FEIBA NF (Anti-Inhibitor Coagulant Complex), nanofiltered and vapor heated, is made from human plasma. Because this product is made from human blood, it may carry a risk of transmitting infectious agents, e.g., viruses, and theoretically, the variant Creutzfeldt-Jakob disease (vCJD) agent. There is also the possibility that unknown infectious agents may be present in such products. The risk that such products will transmit viruses has been reduced by screening plasma donors for prior exposure to certain viruses, by testing for the presence of certain current virus infections, and by inactivating and removing certain viruses during manufacture. Despite these measures, such products may still potentially transmit disease.
Record the batch number of the product every time FEIBA NF is administered to a patient, and consider appropriate vaccination (against hepatitis A and B virus) of patients who receive FEIBA NF.
ALL infections thought by a physician possibly to have been transmitted by this product should be reported by the physician or other healthcare providers to Baxter Healthcare Corporation, at 1-800-423-2862 (in the U.S.) and/or to FDA Med Watch (1-800-FDA-1088 orwww.fda.gov/medwatch).
PRECAUTIONS
Thrombotic and Thromboembolic Complications
Caution should be used when administering FEIBA VH or FEIBA NF to patients with an increased risk of thromboembolic complications. These include, but are not limited to, patients with a history of coronary heart disease, liver disease, disseminated intravascular coagulation, post-operative immobilization, elderly patients and neonates. In each of these situations, the potential benefit of treatment with FEIBA VH or FEIBA NF should be weighed against the risk of these complications. (see WARNINGS:Thrombotic and Thromboembolic Events)
Patients who receive FEIBA VH or FEIBA NF should be monitored for development of signs or symptoms of DIC, acute coronary ischemia, and signs and symptoms of other thrombotic and thromboembolic events. If clinical signs of intravascular coagulation occur, which include changes in blood pressure, changes in pulse rate, respiratory distress, chest pain and/or cough, the infusion should be stopped promptly and appropriate diagnostic and therapeutic measures are to be initiated.
Laboratory indications of DIC are decreased fibrinogen, decreased platelet count, and/or presence of fibrin-fibrinogen degradation products (FDP). Other indications of DIC include significantly prolonged thrombin time, prothrombin time, or partial thromboplastin time.
Concominant Medications
It has been reported that FEIBA NF and antifibrinolytics have been given simultaneously without complications. No adequate and well-controlled studies of the combined or sequential use of FEIBA NF and recombinant Factor VIIa or antifibrinolytics have been conducted. The possibility of thrombotic events should be considered when systemic antifibrinolytics such as tranexamic acid and aminocaproic acid are used during treatment with FEIBA NF. It is recommended not to use antifibrinolytics until 12 hours after the administration of FEIBA NF.
Discordant Response to Bypassing Agents
Due to patient-specific factors the response to a bypassing agent can vary, and in a given bleeding situation patients experiencing insufficient response to one agent may respond to another agent6.
Anamnestic Responses
Administration of FEIBA NF to patients with inhibitors may result in an initial "anamnestic" rise in inhibitor levels. Anamnestic responses with rise in Factor VIII inhibitor titer have been observed in 20% of the cases (see CLINICAL STUDIES). These anamnestic rises have not been observed to interfere with the efficacy of FEIBA. Upon continued administration of FEIBA NF, inhibitors may decrease over time.
Information for Patients
Inform patients receiving FEIBA NF of the benefits and risks associated with treatment. Advise patients of the early signs of hypersensitivity reactions (see WARNINGS: Anaphylaxis and Hypersensitivity Reactions). Advise patients to discontinue use of the product if these symptoms occur and seek immediate emergency treatment.
Some viruses, such as parvovirus B19 or hepatitis A, are particularly difficult to remove or inactivate at this time. Pregnant women and immune-compromised individuals should be informed of the symptoms of parvovirus B19 (i.e. fever, drowsiness, chills, and runny nose followed about two weeks later by a rash, and joint pain). Inform all patients of the symptoms of hepatitis A infection (i.e. several days to weeks of poor appetite, tiredness, and low-grade fever followed by nausea, vomiting, and upper abdominal pain). Dark urine and a yellowed complexion are also common symptoms of Hepatitis A infection.
Advise patients/caregivers to record the batch number of the product every time FEIBA NF is administered outside a healthcare setting.
Advise patients to report any adverse reactions or problems following FEIBA NF administration to their physician or healthcare provider.
Non-Hemophilic Patients
Non-hemophilic patients with acquired inhibitors against Factors VIII, IX or XII may have both a bleeding tendency and an increased risk of thrombosis at the same time.
Monitoring/Laboratory Tests
- Perform a platelet count at the time of initial use of the product and if anticipated treatment responses are not achieved. A sufficient number of functionally intact platelets is considered to be necessary for the efficacy of the product.
- No direct measure of hemostatic efficacy with bypassing agents is available. Coagulation tests such as whole blood clotting time (WBCT), aPTT and TEG may not correlate with clinical improvement. For this reason, attempts at normalizing these values by increasing the dose of FEIBA NF may not be successful and are strongly discouraged because of the potential hazard of producing DIC by overdose.
Drug Interactions
No compatibility studies have been performed with FEIBA NF. Therefore, FEIBA NF must not be mixed with other medicinal products or solvents. (see Concomitant Medications).
Pregnancy Category C
The safety of FEIBA NF during pregnancy has not been established. Animal reproduction studies have not been conducted with FEIBA NF. It is also not known whether FEIBA NF can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. Physicians should carefully consider the potential risks and benefits for each specific patient before prescribing FEIBA NF.Pregnancy and the postpartum period are characterized by an increased risk of thrombosis, and several complications of pregnancy are associated with an increased risk of DIC.
Nursing Mothers
It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when FEIBA NF is administered to a nursing woman. Physicians should carefully consider the potential risks and benefits for each specific patient before prescribing FEIBA NF.
ADVERSE REACTIONS
FEIBA NF can precipitate allergic-type hypersensitivity reactions; these reactions can be severe and can be systemic. Other infusion reactions, such as chills, pyrexia, and hypertension have also been reported.
Adverse Reactions From Clinical Trials
The adverse reactions presented in this section have been reported from two studies with FEIBA for the treatment of bleeding episodes in pediatric and adult patients with hemophilia A or B and inhibitors to factors VIII or IX. One study also enrolled acquired hemophilia patients with factor VIII inhibitors (4 of 49 patients).
| System Organ Class (SOC) | Preferred MedDRA Term |
|
BLOOD AND LYMPHATIC SYSTEM DISORDERS | Increase of inhibitor titer (anamnestic response)† |
| NERVOUS SYSTEM DISORDERS |
Somnolence Dizziness Dysgeusia Hypoesthesia |
| RESPIRATORY, THORACIC, AND MEDIASTINAL DISORDERS | Dyspnea |
| GASTROINTESTINAL DISORDERS | Nausea |
| GENERAL DISORDERS AND ADMINISTRATION SITE CONDITIONS |
Chills Pyrexia Chest pain Chest discomfort |
Post-marketing Adverse Reactions
The following adverse reactions have been reported in the post-marketing experience, listed by MedDRA System Organ Class (SOC), then by Preferred Term in order of severity, where feasible. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
BLOOD AND LYMPHATIC SYSTEM DISORDERS: Disseminated intravascular coagulation
IMMUNE SYSTEM DISORDERS: Anaphylactic reaction, Hypersensitivity
NERVOUS SYSTEM DISORDERS: Paresthesia, Thrombotic stroke, Embolic stroke, Headache
CARDIAC DISORDERS: Myocardial infarction, Tachycardia
VASCULAR DISORDERS: Thrombosis, Venous thrombosis, Arterial thrombosis, Hypotension, Hypertension, Flushing
RESPIRATORY, THORACIC, AND MEDIASTINAL DISORDERS: Pulmonary embolism, Bronchospasm, Wheezing, Cough
GASTROINTESTINAL DISORDERS: Vomiting, Diarrhea, Abdominal discomfort
SKIN AND SUBCUTANEOUS TISSUE DISORDERS: Angioedema, Urticaria, Pruritus, Rash
GENERAL DISORDERS AND ADMINISTRATION SITE CONDITIONS: Malaise, Feeling hot, Injection site pain.
OVERDOSAGE
The risk of thrombotic and thromboembolic events (including DIC, myocardial infarction, venous thrombosis, and pulmonary embolism) may be increased with high doses of FEIBA NF. Some of the reported events occurred with doses above 200 U/kg or with patients with other risk factors for thromboembolic events.
DOSAGE AND ADMINISTRATION
Treatment should be initiated and supervised by a physician experienced in the management of hemophilia.
Clinical trials 1, 2demonstrated that the response to treatment with FEIBA may differ from patient to patient with no correlation to the patient's inhibitor titer. Response may also vary between different types of hemorrhage (e.g. joint hemorrhage vs. CNS hemorrhage). As a general guideline, a dosage range of 50 to 100 Units of FEIBA NF, per kg of body weight is recommended. However, care should be taken to distinguish between the following four indications:
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| Indication | Units/kg of Body Weight | Recommended Dosing Interval | Additional Information |
| Joint Hemorrhage | 50 - 100* | 12 hours |
Continue treatment until clear signs of clinical improvement appear (e.g., relief of pain, reduction of swelling or mobilization of the joint). Two administrations of 100 units/kg a day or a daily total dose of 200 units/kg should not normally be exceeded†. |
| Mucous Membrane Bleeding | 50 – 100* | 6 hours |
Carefully monitor patient (i.e., examine for cecessation of visible bleeding) and perform repeated measurements of the patient's hemoglobin/hematocrit. Two administrations of 100 units/kg a day or a daily total dose of 200 units/kg should not be exceeded†. |
| Soft Tissue Hemorrhage (e.g., retroperitoneal bleeding) | 100 | 12 hours | A daily total dose of 200 units/kg should not be exceeded†. |
| Other Severe Hemorrhage (e.g., CNS bleeds) | 100 | 6-12 hours |
May be indicated at 6-hour intervals until clear clinical improvement is achieved. Single doses of 100 units/kg body weight and a daily dose of 200 units/kg body weight should not be exceeded unless the severity of bleeding warrants and justifies the use of higher doses†. |
Reconstitution
FEIBA NF contains no preservatives. Aseptic technique should be used throughout the entire reconstitution process and the solution should then be used immediately.
- Allow the unopened vials of FEIBA NF (concentrate) and Sterile Water for Injection (diluent) to reach room temperature (not above 37°C, 98°F).
- Remove caps from the concentrate and diluent vials to expose central portions of the rubber stoppers.
- Disinfect the rubber stoppers of both vials using a germicidal solution. Place the vials on an even surface and allow them to dry.
- Open the package of BAXJECT device by peeling away the lid without touching the inside (Fig. A).
- Do not remove the device from the package. Turn the package over and insert the plastic spike through diluent stopper. (Fig. B).
- Grip the package at its edge and pull the package off the device (Fig. B).
- Turn the system over, so that the vial is on top. Quickly insert the other plastic spike into the FEIBA NF stopper (Fig. C). The vacuum will draw the diluent into the FEIBA NF vial. Please make sure that the connection of the two vials should be done expeditiously to close the open fluid pathway created by the first insertion of the spike to the diluent vial.
- Swirl gently until FEIBA NF is completely dissolved. Make sure that FEIBA NF has been dissolved completely; otherwise, active material will not pass through the device filter.
Fig A
Fig B
Fig C
Do not refrigerate after reconstitution!
After complete reconstitution of FEIBA NF its injection or infusion should be commenced as promptly as practicable, but must be completed within three hours following reconstitution. The solution must be given by intravenous injection or intravenous drip infusion.
Rate of Administration:
The maximum injection or infusion rate must not exceed 2 units per kg of body weight per minute. For a patient with a body weight of 75 kg, this corresponds to an infusion rate of 2.5 - 7.5 mL per minute depending on the number of units per vial (see label on vial).
Intravenous Injection or Infusion:
- Inspect for particulate matter and discoloration after reconstituting the concentrate as described under Reconstitution prior to administration. The appearance of the solution should be colorless to slightly yellowish and essentially free of visible particles. Do not use solutions that are cloudy or have deposits.
- Mixing of FEIBA NF with other products or substances must be avoided. It is advisable to flush venous access lines with isotonic saline prior to and after infusion of FEIBA NF.
- If devices other than those supplied with FEIBA NF are used, ensure use of an adequate filter.
- Plastic Luer lock syringes are recommended for use with this product since protein such as FEIBA NF tends to stick to the surface of all-glass syringes.
- Turn the BAXJECT device handle down towards the FEIBA NF concentrate vial and remove the cap attached to the syringe connection of the BAXJECT device (Fig. D).
- Draw air into the syringe, connect the syringe to the BAXJECT device, inject air into the concentrate vial (Fig. E).
- While keeping the syringe plunger in place, turn the system upside down (concentrate vial now on top). Draw the concentrate into the syringe by pulling the plunger back slowly (Fig. F).
- Turn the BAXJECT handle to its original position (facing side way).
- Disconnect the syringe, attach a suitable needle and inject or infuse intravenously as instructed under Rate of Administration.
.
Fig D
Fig E
Fig F
HOW SUPPLIED
FEIBA NF is available in single-dose vials in the following nominal dosage strengths:
Blue - 500 Units per vial (NDC 64193-223-02)
Green - 1000 Units per vial (NDC 64193-224-02)
Purple - 2500 Units per vial (NDC 64193-225-02)
The number of Units of Factor VIII inhibitor bypassing activity is stated on the label of each vial.
FEIBA NF is packaged with a suitable volume (20 mL or 50 mL) of Sterile Water for Injection, U.S.P., one BAXJECT Needleless Transfer Device, and one Package Insert.
The 50 mL SWFI stoppers are not latex-free and may contain Dry Natural Rubber Latex.
Storage
Store at room temperature, not to exceed 25°C (77°F).
Avoid freezing, which may damage the diluent vial.
Store in the original package in order to protect from light.
REFERENCES
- Sjamsoedin L. J. M., Heijnen L., Mauser-Bunschoten E. P., van Geijlswijk J. L., van Houwelingen H., van Asten P., Sixma J. J.: The Effect of Activated Prothrombin-Complex Concentrate (FEIBA) on Joint and Muscle Bleeding in Patients with Hemophilia A and Antibodies to Factor VIII. The New Engl. J. of Med. 305: 717, 1981.
- Hilgartner M. W., Knatterud G. AND THE FEIBA STUDY GROUP: The Use of Factor-Eight-Inhibitor-By-Passing-Activity (FEIBA IMMUNO) Product for Treatment of Bleeding Episodes in Hemophiliacs with Inhibitors. Blood 61: 36, 1983.
- Vermylen J., Schetz J., Semeraro N., Mertens F., Verstraete M.: Evidence that 'Activated' Prothrombin Concentrates Enhance Platelet Coagulant Activity. Brit. J. Haematol. 38: 235, 1978.
- Semeraro N., Vermylen J.: Evidence that Washed Human Platelets Possess Factor-X Activator Activity. Brit. J. Haematol. 36: 107, 1977.
- Wensley R. T.: General Summary of the Use of FEIBA in Haemophiliacs with Inhibitors to FVIII. Presentation at the Second Workshop on Factor VIII Inhibitor Patients, Vienna, 1979.
- Astermark, J., Donfield, S.M., DiMichele, D.M., Gringeri, A., Gilbert, S.A., Waters, J. and Berntorp, E.: A randomized comparison of bypassing agents in haemophilia complicated by an inhibitor: the FEIBA NovoSeven Comparative ( FENOC) Study.: Blood, 109:546, 2007.
To enroll in the confidential, Industry-wide Patient Notification System,
Call 1-888-UPDATE U(1-888-873-2838).
Baxter, Feiba and Prothromplex are trademarks of Baxter AG, Vienna, Austria. Baxter, Feiba and Baxject are trademarks of Baxter International Inc., registered in the U.S. Patent and Trademark Office.
Baxter Healthcare Corporation
Westlake Village, CA 91362 USA
U.S. License No. 140
Revised Feb 2011
Principle Display Panel
FEIBA NF 500U vial label
20 mL size, dried
NDC 64193-323-01
Anti-Inhibitor Coagulant Complex
FEIBA NF
Nanofiltered & Vapor Heated
Baxter
For Intravenous Use Only
Contains no preservative
Dosage & Administration: See accompanying package insert
Storage: Store at room temperature not to exceed 25°C (77°F).
Reconstitution: Use 20 mL sWFI, U.S.P.; Keep at room temperature not to exceed 25°C (77°F); Use within 3 hours of reconstitution
Rx only
FEIBA NF 500U unit carton
20 mL size, dried
NDC 64193-223-02
Anti-Inhibitor Coagulant Complex
FEIBA NF
Nanofiltered & Vapor Heated
Baxter
For Intravenous Use Only
Contains no preservative
Dosage & Administration: See accompanying package insert
Storage: Store at room temperature not to exceed 25°C (77°F). Store in the original package in order to protect from light.
Reconstitution: Use 20 mL sWFI, U.S.P.; Keep at room temperature not to exceed 25°C (77°F); Use within 3 hours of reconstitution
Do Not Freeze
Rx only
Includes BAXJECT Needleless Transfer Device
20 mL Sterile Water for Injection
1A7141
NDC 0338-0764-02
20 mL Single-Dose Container Nonpyrogenic
Sterile Water for Injection, USP
for reconstitution of accompanying product
Do not use unless clear. No antimicrobial agent or other substance has been added. Do not use for intravascular injection without making approximately isotonic by addition of suitable solute. Discard unused portion. Rx Only. This Product Contains Dry Natural Rubber.
Baxter
Manufactured by
Baxter Healthcare Corporation
Deerfield, IL 60015 USA
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| Labeler - Baxalta Incorporated (085206634) |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Baxter Aktiengesellschaft | 300434670 | MANUFACTURE | |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Baxter Healthcare Corporation | 001728059 | MANUFACTURE | |