Web2 feb. 2024 · Feb 2, 2024. Tim Smith. This week, the FDA announced that 27 lots of levothyroxine sodium oral solution, used for hypothyroidism, were being recalled due to potentially being subpotent. The FDA announced that pharmaceutical company IBSA Pharma recalled 27 lots of levothyroxine sodium (TIROSINT-SOL) oral solution due to … Web7 mrt. 2024 · Photo: Sarah Silbiger/Getty Images. Select eye drops have been recalled over concerns the products may not be sterile, notices posted on the Food & Drug Administration website show. Why it matters: The recall notices for select lots of Purely Soothing 15% MSM Drops and Brimonidine Tartrate Ophthalmic Solution did not list any illnesses or ...
Drug Safety Alerts and Warnings - ASHP
WebPatients prescribed angiotensin II receptor medications have filed Losartan recall lawsuits against drug manufacturers. Doctors regularly prescribed antihypertensive drugs like Losartan, Valsartan, and Irbesartan to millions of patients in the United States and worldwide.The FDA found that more than a dozen manufacturers produced prescription … Web23 mrt. 2024 · CNN —. Pfizer has issued a recall for a high blood pressure medication distributed under three names, according to the company. Accuretic and its two generic … sigma touche clavier
FDA cautions manufacturers of plant-based proteins to remember ...
Web15 dec. 2024 · Quinapril Shortage 2024 – Alternatives and Recall. 15 Dec 2024. Why there is Quinapril shortage? The Therapeutic Goods Administration ( TGA) investigates the possible contamination of several products. The doctors are urged to talk to their patients about alternative blood pressure-lowering treatments to quinapril because of the shortage. Web13 uur geleden · By Coral Beach on April 14, 2024. The Food and Drug Administration is reminding manufacturers of plant-based proteins to be aware of the legal requirements of such products. The reminder is a pre ... Web7 apr. 2024 · Link Copied! Certain Philips DreamStation CPAP and BiPAP machines are being recalled. The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for ... the priority focus of community development