An FDA panel has voted in favor of the safety and effectiveness of Paxlovid for COVID-19.
All articles by Diana Ernst, RPh
This age group is now eligible to receive the booster dose at least 2 months after they complete primary vaccination with 3 doses of the monovalent vaccine.
Results showed a significantly greater proportion of patients treated with tapinarof cream achieved vIGA-AD success compared with vehicle cream.
The approval was supported by data from the randomized, double-blind, placebo-controlled phase 3 LAVENDER study.
Earlier this month, Global Pharma Healthcare had announced a nationwide recall of its artificial tear lubricant eye drops distributed by EzriCare, LLC and Delsam Pharma.
Tepezza, a fully human monoclonal antibody, is approved for the treatment of thyroid eye disease.
The BLA submission is based on positive results across four phase 3 studies in wet AMD and DME.
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