There is a new warning about this raised pain for sale in the management of the FDA.

Make sure to check your wardrobe for this recalled medicine.


YourThe drug furniture is probably filled With various analgesics of pain and medicine on the counter (OTC) waiting for each time you need it, but there may also be hidden hidden dangers. It is important to check your medications in light of new warnings of the US and Drug Administration (FDA) on drugs that can endanger you. In fact, a recent announcement of the FDA mentions one of the most commonly used painful pain analgesics. Read it to see if you have this medicine in your wardrobe and for more medicines to avoid,If you take this medicine, American officials have a new warning for you.

The FDA announced a reminder for nearly 200,000 acetaminophen bottles.

acetaminophen recall
FDA

FDA announced on April 2nd that A-S, LLM (ASM) drug solutionsrecalling voluntarily nearly 200,000 bottles acetaminophen of 500 tablets of 500 milligrams. The recalled medicine came in white bottles at 100 plastic accounts and has been included in essential health kits distributed to members of Humana, an American health insurance company. These kits also included a hand disinfectant bottle, a reusable facial mask, a bag of cough drops, a digital thermometer and 50 disposable gloves. And for more acetaminophen dangers,If you take Tylenol with that, your liver is in danger, say experts.

The drug has been recalled because of a malla lambling.

senior man with his medicine bottles
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According to the FDA, these bottles are recalled as they "contain an incomplete prescription drug label rather than the brand required on the facts of the OTC drug." Drugs, which were probably distributed nationally between January 14 and March 15, have only a short RX drug label outside the bottle, which "lack of the complete diagram of the facts of Free-up drug ", according to the announcement of the reminder. The FDA indicates Gestion drugs at TBT thatAdhere to the drug facts label must include the following information: the active ingredients of the product, including the amount of each dosage unit; the purpose of the product; uses (indications) for the product; Specific warnings, including when the product should not be used under any circumstances and when appropriate to consult a physician or pharmacist; dosage instructions; and the inactive ingredients of the product.

According to a declaration by Humana, about 16,000 Humana members received poorly clear bottles. "It is important to note that all essential health kits were not affected and that the recall was not related to the safety of the drug itself. Instead, bottles provided by drug solutions were not properly labeled for freely use "a spokesman for Humana saidBetter life. And for more useful information delivered directly in your inbox,Sign up for our daily newsletter.

This label can help prevent serious complications.

Close up young woman pouring pills out of bottle. Stressed millennial student holding aspirin painkiller antidepressant antibiotic to relieve pain, feeling unhealthy at home or office.
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Without an appropriate warning label, this TBT drug could be misused with unfortunately. For example, if consumers take more than the recommended dose of acetaminophen (which should be included on the label), they may be at risk of liver damage. The FDA also notes that consumers should be aware if they are allergic to an active ingredient of this medicine, which would also be registered on a full label. According to the FDA, ASM has not yet "received any unwanted event report related to this reminder". And for more warnings of the FDA,If you have these supplements at home, the FDA says "destroy them".

Customers who have this product are invited to return it.

Young man using tablet for pharmaceutical questions
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The FDA asserts that ASM notifies its distributors and customers by mail and organize the return of all recalled products. If you have this product, ASM asks you that you "stop using it and returning it into pre-addressed return shipments that will be provided by ASM or distributors." If you have any questions, you can contact ASM Customer Service, and if you have problems, you think that the use of this recalled medicine, you need to talk to your doctor or health care provider. The FDA also requests that all "unwanted reactions or problems of proven quality with the use of this product" be reported to theFDA MedWatch Adverse Event Reports program. And for more OTC drug concerns,If you take this grateful medicine more than twice a week, consult a doctor.


Categories: Health
Tags: medicine / News
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