July 24, 2020
July 24, 2020 – The U.S. FDA has approved Onureg® (azacitidine) tablets, manufactured by Bristol-Myers
Squibb, to provide continued treatment for adults diagnosed with acute myeloid
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July 24, 2020
July 24, 2020 – The U.S. FDA has approved Breztri AerosphereTM (budesonide/glycopyrrolate/formoterol fumarate), manufactured by AstraZeneca, to provide maintenance treatment
July 24, 2020
July 24, 2020 – The U.S. FDA has approved an expanded indication for VecticalTM (calcitriol) topical
ointment, manufactured by Galderma Laboratories, to treat mild to
July 1, 2020
July 31, 2020 – The U.S. FDA has approved an expanded indication for Evotaz® (atazanavir/cobicistat) oral
tablets, manufactured by Bristol-Myers Squibb, to include its use in
July 1, 2020
July 31, 2020 – The U.S. FDA has approved a new indication for Epidiolex® (cannabidiol) oral solution,
manufactured by GW Pharmaceuticals. The drug is now indicated to
July 1, 2020
July 31, 2020 – The U.S. FDA has approved an expanded indication for Prezcobix® (darunavir/cobicistat)
oral tablets, manufactured by Janssen Pharmaceuticals. The product is
June 18, 2020
June 18, 2020 – The U.S. FDA has approved a new indication for Crysvita® (burosumab), manufactured by
Ultragenyx and Kyowa Kirin. The drug is now indicated to treat patients who are
June 17, 2020
June 17, 2020 – The U.S. FDA has approved a new indication for Keytruda® (pembrolizumab) injection,
manufactured by Merck. The drug is now indicated to treat adult and pediatric