Emicizumab(Hemlibra)
Acetylcysteine Injection, FLUIMUCIL, Acetylcysteine InjectionAcetylcysteine Injection, FLUIMUCIL, Acetylcysteine InjectionAcetylcysteine Injection, FLUIMUCIL, Acetylcysteine Injection
Reference price:
Manufacturer:
Pfizer Inc.
Formulation:
INJECTION
Validity period:
24 months
Reminder: The outer packaging is for reference only, please purchase and use under the guidance of a pharmacist. For read by medical and pharmaceutical professionals only.

Hemlibra(Emicizumab) Instructions:Uses,Dosage, Side Effects

HEMLIBRA is a bispecific monoclonal antibody used for prophylactic treatment in hemophilia A patients.

Introduction to HEMLIBRA

HEMLIBRA (emicizumab-kxwh) is a subcutaneous injection designed to prevent bleeding episodes in patients with hemophilia A, with or without factor VIII inhibitors. It works by bridging factor IXa and factor X to restore clotting function. Available in multiple dosage strengths, it offers flexible dosing regimens for long-term management.

Generic name

Emicizumab(Hemlibra)
English name
Emicizumab
Alternative Names
Hemlibra
Drug prices
Indications

HEMLIBRA is indicated for routine prophylaxis in adult and pediatric patients (newborn and older) with congenital hemophilia A (Factor VIII deficiency), regardless of inhibitor status.

Therapeutic Target
Bispecific monoclonal antibody targeting Factor IXa and Factor X to restore the function of missing activated Factor VIII (FVIIIa)
Active Ingredients
Emicizumab
Dosage form
INJECTION
specifications
30mg/1mL/box
Description
Dosage and Administration

1. Loading Dose: 3 mg/kg subcutaneously once weekly for the first 4 weeks.

2. Maintenance Dose: Choose one of the following regimens:

1.5 mg/kg once weekly, or

3 mg/kg once every two weeks, or

6 mg/kg once every four weeks.

3. Discontinue prophylactic bypassing agents one day prior to initiating HEMLIBRA.

4. Factor VIII prophylaxis may be continued during the first week of HEMLIBRA therapy.

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