August 10, 2021 – SterRx, LLC, has recalled three lots of Sodium Bicarbonate in 5% Dextrose Injection 150mEq per 1,000mL to the hospital pharmacy level as a result of waterborne
August 6, 2021 – The U.S. FDA has approved Sanofi’s Nexviazyme® (avalglucosidase alfa-ngpt), to treat
late-onset Pompe disease (LOPD) in patients who are at least a year old.
August 6, 2021 – KVK Tech, Inc., has voluntarily recalled two lots of Atovaquone Oral Suspension, USP 750
mg/5mL, following customer complaints that the product was unusually gritty
August 2, 2021 – The U.S. FDA has approved SaphneloTM (anifrolumab-fnia), manufactured by AstraZeneca,
to treat moderate to severe systemic lupus erythematosus (SLE) in adults who
July 30, 2021
July 30, 2021 – The U.S. FDA has updated emergency use authorization (EUA) for Regeneron’s REGEN-
COVTM (casirivimab and imdevimab). The monoclonal antibody
July 29, 2021 – Nucala® (mepolizumab), manufactured by GlaxoSmithKline, has received U.S. FDA approval for a new indication to treat chronic rhinosinusitis with nasal polyps (CRSwNP)
July 28, 2021 – Pepaxto® (melphalan flufenamide – Oncopeptides AB) may increase the risk of death for patients who have multiple myeloma, according to the U.S. FDA. In 2021