Guest guest Posted January 13, 2011 Report Share Posted January 13, 2011 FDA MedWatch Alert Sent to subscribers of: acetaminophen/codeine systemic, acetaminophen/hydrocodone systemic, acetaminophen/oxycodone systemic Drug Safety Communication: Acetaminophen Prescription Products Limited to 325 mg Per Dosage Unit: January 13, 2011 Audience: Pharmacy, Pain Management. ISSUE: FDA notified healthcare professionals that it has asked drug manufacturers to limit the strength of acetaminophen in prescription drug products, predominantly combinations of acetaminophen and opioids, to 325 mg per tablet, capsule, or other dosage unit, making these products safer for patients. This action will help to reduce the risk of severe liver injury and allergic reactions associated with acetaminophen... Read more... Get these updates via twitter Drugs.com. All rights reserved. Change your notification settings or unsubscribe here. Quote Link to comment Share on other sites More sharing options...
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