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Draft Hemophilia Drug Policies
Draft policies are listed below. If there are no policies listed, it means there are currently no policies in draft status.
Drug policies are based on:
- Information in FDA-approved package inserts (and black box warnings, alerts or other information disseminated by the FDA, as applicable);
- Research of current medical and pharmacy literature; and/or,
- Review of common medical practices in the treatment and diagnosis of disease.
Pharmacy drug policies provide a guide to coverage. Pharmacy policies are not intended to dictate to providers how to practice medicine. Providers should exercise their medical judgment in providing the care they feel is most appropriate for their patients.
Note: Coverage is subject to member's specific benefits. Group-specific policies will supersede these policies, when applicable. Always verify member eligibility and benefits.
Comment on Draft Drug Policies
Participating providers are invited to submit scientific, evidence-based information, professional consensus opinions and other information supported by medical literature relevant to these draft policies for consideration.
Comments are accepted for 45 days from the posting date listed on the draft policy.
Make sure your voice is heard by providing feedback directly to us:
- Complete our online policy feedback form
- Send comments with supporting documentation by mail or fax
Credence Blue Cross and Blue Shield Service Center
Attn: Pharmacy Department
P.O. Box 10447
Birmingham, AL 35202
|Policy #||Policy Title||Print View|
|PH-00340||Hemophilia Products - Factor VIII Prior Authorization Program Summary|
|PH-90344||Hemophilia Products – von Willebrand Factor: Vonvendi®|