The current vaccine schedule in the United States may not be optimal, the Food and Drug Administration’s...
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MONDAY, Aug. 25, 2025 -- The U.S. Food and Drug Administration is suspending the biologics license for the live-attenuated chikungunya vaccine, Ixchiq, in the United States. The move comes after reports of serious side effects in older adults...
The current vaccine schedule in the United States may not be optimal, the Food and Drug Administration’s...
SAN DIEGO – September 25, 2025 – Crinetics Pharmaceuticals, Inc. (Nasdaq: CRNX) today announced that the U.S. Food and Drug Administration...
SAN DIEGO – September 25, 2025 – Crinetics Pharmaceuticals, Inc. (Nasdaq: CRNX) today announced that the U.S. Food and Drug Administration...
TUESDAY, Sept. 30, 2025 -- The U.S. Food and Drug Administration has approved Inluriyo (imlunestrant), an oral estrogen receptor antagonist, for the...
September 25, 2025 -- MEDRx announced that the U.S. Food and Drug Administration (FDA) has approved Bondlido, a lidocaine*1 patch MEDRx Group and D....
The U.S. Food and Drug Administration (FDA)...
Health and Human Services Secretary Robert F. Kennedy Jr. told red-state governors the Food and Drug Administration is conducting a safety review of...
Health and Human Services Secretary Robert F. Kennedy Jr. told red-state governors the Food and Drug Administration is conducting a safety review of...
THURSDAY, Oct. 2, 2025 (HealthDay News) -- The U.S. Food and Drug Administration has approved Tremfya (guselkumab) for the treatment of plaque...
WEDNESDAY, Sept. 24, 2025 -- The U.S. Food and Drug Administration has approved a subcutaneous (SC) induction regimen of Tremfya (guselkumab) for the...