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Carol Eustice

FDA Recommends Discontinuation of Certain Prescription Combination Drugs Used for Arthritis Pain

By January 15, 2014

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acetaminophensafetyOn January 14, 2014, the FDA issued a recommendation to health care professionals: stop prescribing and dispensing prescription combination drug products that contain more than 325 mg. of acetaminophen per tablet, capsule or other dosage unit. According to the FDA, more than 325 mg. acetaminophen per dose does not provide additional benefit that outweighs the additional risks of liver injury.

The FDA claims that limiting the amount of acetaminophen per dose to 325 mg. will reduce the risk of liver injury from inadvertent overdose of acetaminophen which can result in liver failure, liver transplant, or death. Many arthritis patients take prescription combination drugs to relieve pain. If you take a combination product with acetaminophen (e.g., Lortab 10/500, Percocet 7.5/500, or others), read the label to see how much acetaminophen (APAP) is in each pill or dosage unit. If you have questions, talk to your doctor and pharmacist. The new recommendation may require a change to your prescription. The recommendation does not affect over-the-counter acetaminophen products.

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Comments
January 23, 2014 at 2:51 pm
(1) sparkles says:

As if the FFDA really knows it all. They approve garbage drugs for pain, it’s no wonder this has evolved. A responsible adult knows how to monitor pain medication, along with other modaliies. It’s not given to patients that really need it. Treated like a “child’. And, they make it like they don’t have there hands in the pot!

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