FDA: Acetaminophen Overuse May Cause Liver Damage

A bottle filled with aspirin tabletsYou’re in pain. You pop a vicodin. Then another pain pill. And another. And another.

But…do you really know how much acetaminophen particularly in combination with other prescriptions, you should be taking to avoid not only pain, but dangerous side effects you weren’t counting on?

READ: Aspirin vs. Acetaminophen

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The Food and Drug Administration (FDA) has asked doctors not to prescribe combination drugs containing more than 325 mg of acetaminophen, as higher doses increase the risk of liver damage, or even death.

“Many consumers are often unaware that many products (both prescription and OTC) contain acetaminophen, making it easy to accidentally take too much,” the FDA said in a statement.

READ: Why The FDA Wants To Restrict…

The warning applies to all medication, including over-the-counter drugs such as Tylenol, which contains acetaminophen.

Acetaminophen is often used in pain medications with opioids such as oxycodone (Percocet), hydrocodone (Vicodin) and codeine (Tylenol with Codeine). These are called combination drugs, and the Food and Drug Administration is asking doctors to stop prescribing those that have more than 325 mg of acetaminophen per dose.

In 2011, the FDA had asked manufacturers of prescription combination drugs, medication containing two or more drugs, to stop manufacturing drugs containing more than 325 mg of acetaminophen. While more than half of the manufacturers complied, there are still drugs available continuing a high dosage of acetaminophen.

READ: Is An Aspirin A Day Still A Good Idea?

The federal agency says it plans to start the process of withdrawing approval of prescription combination drugs from manufacturers that have not complied.

The FDA has set the recommended maximum for adults at 4,000 milligrams per day. Additionally, consumers should not take more than the prescribed dose of any medication that contains acetaminophen, and should avoid taking more than one acetaminophen product at a time.

If you have questions about any medications, talk to your doctor or a pharmacist.

Kraft Velveeta Recall Issued

Cheesy beef dinner in a skilletTruitt Brothers is recalling more than a million pounds of a Kraft Velveeta product for failing to identify soy as an ingredient, the U.S. government announced on Monday.

READ: Aldi U.K. Confirms Up To 100% Horsemeat In Selected Beef Products

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READ: Top Recalled Foods Of 2013

The U.S. Department of Agriculture’s Food Safety and Inspection Service said that manufacturer Truitt Brothers is recalling 1.77 million pounds of Kraft Velveeta Cheesy Skillets Singles – Ultimate Cheeseburger Mac. The macaroni and cheese product contains pasta and ground beef.

READ: Packaged Salad: Convenient Or Contaminated?

Some of the labels do not mention the presence of hydrolyzed soy protein and dried soy sauce, which are allergens.
“The inaccurate labeling is the only thing wrong with the product,” said Kraft Foods spokeswoman Joyce Hodel. “If an individual has no allergies or sensitivities to soy, then the product is perfectly safe to consume.”

READ: You Are Being Poisoned

The recall applies to food with a sale date from March 2, 2014 to October 23, 2014. It does not apply to other Kraft or Velveeta products, according to the government.