Viibryd approval

January 24, 2011

THE US Food and Drug Administration has approved Viibryd tablets (vilazodone hydrochloride) for the treatment of major depressive disorder in adults. Available in 10, 20 and 40mg tablets, the drug’s most common side effects include diarrhea, nausea, vomiting, and insomnia. MEANWHILE the FDA has also unveiled its 2011 plan to improve the most common path to market for medical devices. Key actions featured in the plan include streamlining the “de novo” review process for certain innovative, lower-risk medical devices; clarifying when clinical data should be submitted in a premarket submission; and establishing a new Center Science Council of FDA experts to ensure timely and consistent science-based decision making. See www.fda.gov for details.

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Pharmacy Daily | Viibryd approval

Viibryd approval

Other recent headlines

Expanded prescribing for Vic pharmacists

DDI alerts: more harm than good?

Tas govt funds training for expanded scope

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES