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Education for your patients
Novo Nordisk helps support your patients with resources and tools to manage hemophilia A, right from the start.
Education for your patients
Novo Nordisk helps support your patients with resources and tools to manage hemophilia A, right from the start.
Share these resources with your patients
Getting Started For Patients
Esperoct.com provides a step-by-step overview about the process of starting with Esperoct®, from ordering factor to scheduling an infusion.
Help patients get started by directing them to esperoct.com/starting-treatment/get-started
Education for you
Explore Esperoct® product information and learn how it works.
Support for treatment costs
See what programs we offer for financial support.
Selected Important Safety Information
Contraindications
- Do not use in patients who have known hypersensitivity to Esperoct® or its components, including hamster proteins
Warnings and Precautions
- Hypersensitivity reactions, including anaphylaxis, may occur. Should hypersensitivity reactions occur, discontinue Esperoct® and administer appropriate treatment
Indications and Usage
Esperoct® [antihemophilic factor (recombinant), glycopegylated-exei] is indicated for use in adults and children with hemophilia A for on-demand treatment and control of bleeding episodes, perioperative management of bleeding, and routine prophylaxis to reduce the frequency of bleeding episodes
- Esperoct® is not indicated for the treatment of von Willebrand disease
Important Safety Information
Contraindications
- Do not use in patients who have known hypersensitivity to Esperoct® or its components, including hamster proteins
Warnings and Precautions
- Hypersensitivity reactions, including anaphylaxis, may occur. Should hypersensitivity reactions occur, discontinue Esperoct® and administer appropriate treatment
- Development of neutralizing antibodies (inhibitors) has occurred. Perform an assay that measures Factor VIII inhibitor concentration if bleeding is not controlled with the recommended dose of Esperoct® or if the expected plasma Factor VIII activity levels are not attained
Adverse Reactions
- The most frequently reported adverse reactions in clinical trials (≥1%) were rash, redness, itching (pruritus), and injection site reactions
Please click here for Prescribing Information.