Farydak Approved for Multiple Myeloma
The U.S. Food and Drug Administration (FDA) approved Farydak (panobinostat), manufactured by Novartis. Farydak is used for the treatment of patients with multiple myeloma who have received at least two prior regimens including Velcade (bortezomib – Takeda) and an immunomodulatory agent. The recommended dose of Farydak is 20mg taken orally once every other day for three doses per week of Weeks 1 and 2 of each 21-day cycle for eight cycles and is to be given in combination with Velcade and dexamethasone. Novartis plans on launching Farydak by the end of March through a limited network of specialty pharmacies.
Adverse reactions or quality problems experienced with the use of a recalled product may be reported to the FDA’s MedWatch Adverse Event Reporting Program either online, by regular mail or by fax.
- Complete and submit the report Online: www.fda.gov/medwatch/report.htm
- Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
Actual drug patent expiration dates and a availability of new medications are subject to change due to patent litigation, settlement agreements, additional patents, exclusivities, and final FDA approval. Distribution and availability of new medications at pharmacies may not occur immediately following FDA approval. Patients are advised to speak with their healthcare professional or pharmacist regarding appropriateness as well as actual availability.
*This is provided for information only. The reference to any medication above does not mean the medication is covered by your plan.