Pradaxa label updated with contraindication
The anticoagulant dabigatran etexilate mesylate should not be used in patients with mechanical prosthetic heart valves, the FDA warns.
The anticoagulant dabigatran etexilate mesylate should not be used in patients with mechanical prosthetic heart valves, the FDA warns.
A boxed warning about potentially fatal skin reactions will be added to the oral hepatitis C drug telaprevir.
The FDA is warning against taking sodium oxybate with alcohol or CNS depressant drugs, due to increased risk for impaired consciousness and respiratory distress.
Heparin label changes eliminate the need for clinicians to calculate the total amount of heparin medication in a product containing more than 1 mL.
Health officials have confirmed the presence of the fungus Exserohilum rostratum in unopened recalled steroid vials from New England Compounding Pharmacy.
Although no new exposures to contaminated meds are likely, the CDC is urging clinicians to remain on the look out for new cases in the coming weeks.
The FDA has approved a risk evaluation and mitigation strategy (REMS) for extended-release (ER) and long-acting (LA) opioids.
The FDA has issued a Federal Register notice instructing companies to stop manufacturing and distributing certain unapproved drugs that contain oxycodone.
Patients often consider supplements and herbs harmless, but combining them with other drugs can have devastating consequences.
The FDA is warning against using Reumofan Plus, a Mexican product marketed as a “natural” dietary supplement for pain relief, because it may contain unlabeled, potentially harmful pharmaceuticals.