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Tretten

Generic name: Coagulation Factor XIII A-Subunit (Recombinant)
Drug class: Miscellaneous coagulation modifiers
Approval date: December 23,2013
Company: Novo Nordisk A/S

Medically reviewed by Drugs.com. Last updated on Aug 23, 2023.

Treatment for: Factor XIII A-Subunit Deficiency

FDA Approves Tretten

The U.S. Food and Drug Administration (FDA) has approved Tretten (Coagulation Factor XIII A-Subunit [Recombinant]) for the routine prophylaxis of bleeding in people with congenital factor XIII (FXIII) A-subunit deficiency.

Tretten Petient Information

This leaflet summarizes important in formation about Tretten. Please read it carefully before using Tretten and each time you get a refill because there may be new information provided. This information does not take the place of talking with your healthcare provider, and it does not include all of the important information about Tretten.

If you have any questions after reading this, ask your healthcare provider.

What is Tretten?

Tretten is an injectable medicine used to prevent bleeding in adults and children who have congenital factor XIII (FXIII) A-subunit deficiency. Tretten is man-made and does not contain animal or human materials.

Who should not use Tretten?

You should not use Tretten if you have ever had allergic (hypersensitivity) reactions, including severe, whole body reaction (anaphylaxis) to Tretten or any of the ingredients.

What should I tell my healthcare provider before Tretten is given?

Tell your healthcare provider about all of your medical conditions, including:

Tell your healthcare provider about all of the medicines you take, including all prescription and non-prescription medicines such as over-the-counter medicines, supplements, or herbal remedies.

How is Tretten given?

Tretten is given as an injection into your vein (intravenous injection). These injections are given once a month. Your dose will depend on your body weight. Use the dose that your healthcare provider has prescribed for you based on your weight. Before injecting Tretten, it must be dissolved (reconstituted) using the sterile water that is provided in the package. Throw away any Tretten left in the vial after you inject your dose because it may become unsterile.

Tretten side effects

Call your healthcare provider or go to the emergency department right away if you have any of the following symptoms after using Tretten:

Other possible side effects may include:

These are not all the possible side effects of Tretten. Tell your healthcare provider about any side effect that bothers you or that does not go away. You can also report side effects to the Food and Drug Administration (FDA) at 1-800-FDA-1088.

How should I store Tretten?

It is important to store Tretten correctly.

Before preparing Tretten for injection

After preparing Tretten for injection (reconstituted)

What else should I know about Tretten?

Do not use Tretten for a condition for which it is not prescribed. Do not share Tretten with other people,even if they have the same symptoms that you have.

Talk to your healthcare provider if you would like more information.

Tretten ingredients include:

Tretten and the sterile water vials provided in the package are not made with natural rubber latex.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.