FDA Drug Alerts

Get the latest drug alerts and warnings issued by the FDA and published on

[FDA Drug Alerts @DrugscomAlerts]

Unique Pharmaceutical Laboratories Issues Voluntary Nationwide Recall of Cetirizine Hydrochloride Tablets USP 5 mg Due to Potential Cross Contamination with Ranitidine https://t.co/lsIeQPo2Iz

[FDA Drug Alerts @DrugscomAlerts]

FDA Alerts Health Care Providers to Cases of Neurologic Complications from General Anesthesia Linked to Genetic Variant in Patients of Maternal Venezuelan Ancestry https://t.co/zeWhJXfNwP

[FDA Drug Alerts @DrugscomAlerts]

FDA Approves Labeling Changes for Over-the-Counter (OTC) Weight Loss Drug alli (Orlistat) to Warn of Risk of Kidney Stones and Kidney Injury https://t.co/Ovs1FVO8aq

[FDA Drug Alerts @DrugscomAlerts]

Haleon Issues Voluntary Nationwide Recall of Gas-X Extra Strength Softgels 125mg, 120 ct. and 72 ct. https://t.co/9Frqio4mvV

[FDA Drug Alerts @DrugscomAlerts]

FDA Warns Consumers Not To Use Expired Amazon Basic Care Levonorgestrel 1.5 mg https://t.co/ZHuk6nTn9J

[FDA Drug Alerts @DrugscomAlerts]

Sun Pharma Initiates Recall of DOXOrubicin Hydrochloride Liposome Injection 50mg/25 mL Due To Potential Presence of Glass Particles https://t.co/WukPuaLCji

[FDA Drug Alerts @DrugscomAlerts]

XD Investments LLC Recalls Better Weather Fix Elixir Products Due to Undeclared Mitragynine and Mitragynine Pseuoindoxyl https://t.co/8vj6C8cDnu

[FDA Drug Alerts @DrugscomAlerts]

FDA Safety Alert: Pharmacal Issues Nationwide Recall of MG217 Multi-Symptom Treatment Cream & Skin Protectant Eczema Cream Due to Microbial Contamination https://t.co/agR3uqt6vo

[FDA Drug Alerts @DrugscomAlerts]

FDA Alerts Health Care Providers and Patients About Voluntary Withdrawal of Tazverik (tazemetostat) Due to Increased Risk of New Blood Cancers https://t.co/lBGnrEvaqc

[FDA Drug Alerts @DrugscomAlerts]

B. Braun Medical, Inc. Issues Voluntary Nationwide Recall of Lactated Ringer’s Injection, 1L, E7500 Due to the Presence of Particulate Matter in Solution https://t.co/hjJLGRsBeX

[FDA Drug Alerts @DrugscomAlerts]

Aphreseller Issues Voluntary Recall of Kian Pee Wan Capsules Due the Presence of Undeclared Dexamethasone and Cyproheptadine https://t.co/xKOgSiopmp

[FDA Drug Alerts @DrugscomAlerts]

FDA Identifies Cases of Serious Liver Injury in Patients Taking Tavneos (avacopan) for Severe Active Anti-Neutrophil Cytoplasmic Autoantibody Associated Vasculitis https://t.co/YXzMf065CI

[FDA Drug Alerts @DrugscomAlerts]

Amneal Issues Recall of Magnesium Sulfate in Water for Injection, USP 4 g/100mL (NDC 70121-1720-3) Due to Product Mix-Up https://t.co/npEgsS1HEx

[FDA Drug Alerts @DrugscomAlerts]

FDA Is Requiring Warning about Vitamin B6 Deficiency and Associated Seizures for Drug Products Containing Carbidopa/Levodopa https://t.co/Z0zwFi8Hj1

[FDA Drug Alerts @DrugscomAlerts]

Cardinal Health Issues Voluntary Nationwide Recall of Webcol™ Large Alcohol Prep Pad https://t.co/jWcU9EeQrg

[FDA Drug Alerts @DrugscomAlerts]

FDA Approves Labeling Changes to Six Menopausal Hormone Therapy Products https://t.co/eEixgCo6wA

[FDA Drug Alerts @DrugscomAlerts]

FDA Requests Removal of Suicidal Behavior and Ideation Warning from Glucagon-Like Peptide-1 Receptor Agonist (GLP-1 RA) Medications https://t.co/lHJNxQkDXM

[FDA Drug Alerts @DrugscomAlerts]

FDA Safety Alert: MediNatura New Mexico, Inc. Issues Voluntary Nationwide Recall of ReBoost Nasal Spray Due to Microbial Contamination https://t.co/C5LBkF5sts

[FDA Drug Alerts @DrugscomAlerts]

Novo Nordisk Warns Consumers About Counterfeit Ozempic (semaglutide) Injection 1 mg in the US https://t.co/knDINfr9cs

[FDA Drug Alerts @DrugscomAlerts]

FDA Investigating Death Due to Neutralizing Antibodies to ADAMTS13 following Adzynma Treatment https://t.co/btQvioVcPK