Zemaira® Sample Program
We are pleased to provide the Alpha-1 community with the option of trying Zemaira® at
no charge for up to 2 weeks.* Switching to Zemaira® is easy,
and participation in the Zemaira® Sample Program will not jeopardize
your current Alpha-1 product supply.
How to get your Zemaira® Trial Pack
- Sign up for the Zemaira® Sample
Program. You will receive an e-mail with a Zemaira® Product Sample
Request to take to your doctor and additional information about getting your Trial
Pack.
- Ask your doctor to fill out the Product Sample Request Form and fax it to our
Customer Support group.
- We will ship your Zemaira® Trial Pack directly to your doctor
within 1 week of receiving the request.
- Talk with your doctor to determine how and where you will receive Zemaira® infusions.
If you have any questions or would like more information, please call 1-866-ZEMAIRA
(1-866-936-2472).
Sign up now to experience
Zemaira® for yourself.
Should you decide to continue therapy with Zemaira®, you will be eligible to participate in the Alpha-1 Guardian Program and the CSL Behring AssuranceSM Program.
Important Safety Information
Alpha1-Proteinase Inhibitor (Human), Zemaira® is indicated for chronic augmentation and maintenance therapy for adults with alpha1-proteinase inhibitor (A1-PI) deficiency and emphysema. Clinical data demonstrating the long-term effects of chronic augmentation therapy with Zemaira® are not available.
Zemaira® may not be appropriate for the following adult individuals as they may experience severe reactions, including anaphylaxis: individuals with a known hypersensitivity and/or history of anaphylaxis or severe systemic reaction to A1-PI products or their components, and individuals with selective IgA deficiencies who have known antibodies against IgA.
In clinical studies, the following treatment-related adverse reactions were reported in 1% of subjects: asthenia (fatigue), injection-site pain, dizziness, headache, paresthesia (tingling), and pruritus (itching).
Zemaira® is derived from human plasma. The risk of transmission of infectious agents, including viruses and, theoretically, the Creutzfeldt-Jakob disease (CJD) agent, cannot be completely eliminated.
Please see full prescribing information.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.