Good Lifestyle

There are many different ways to fight against difficult pain, to over -the -counter products For general showers to more powerful prescription drugs for serious discomfort. These drugs can help people feel better and hope to resume a relatively regular routine. But now the US Food & Drug Administration (FDA) warns that a pain medication is recalled due to a potentially serious problem of contamination.

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In an alert published by the agency on March 28, the pharmaceutical company based in New Jersey Eugia US LLC announced that he had started a voluntary reminder of a lot of his methocarbamol injection, 1000 mg / 10 ml USP wrapped in single dose bottles of 10 ml. The affected product is marked with lot 3MC2301, the expiration date November 2026 and the National Drug Code (NDC) 55150-223-10. The company claims that the drug was sent to distributors of the country from January 12, 2024 to January 16, 2024. AE0FCC31AE342FD3A1346EBB1F342FCB

Depending on the notice, the injectable drug is often used with rest and physiotherapy to help comfort patients suffering from "acute and painful musculoskeletal conditions". The company says it was alerted by a customer that small white particles seemed to float in one of the affected bottles.

In some cases, receiving an injection which contains small contaminants can cause irritation and swelling in the zone of the blow. But it can also be much more serious if the particles make their way in the blood circulation, where they can go to vital organs and cause bloodshed blockages in the heart, the lungs or the brain. The opinion warns that this could lead to a stroke and potentially death.

The company says it is notifying all customers of the situation by sending recall letters and organizing all the articles concerned returned and replaced. They warn that hospitals, pharmacies and other institutions that have bottles recalled at hand should stop using them immediately.

The opinion indicates that all customers with recall questions can reach Eugia US LLC from 8:00 a.m. to 5:00 p.m. Eastern standard hour (east) Monday to Friday by calling the 1-866-850-2876 and in Selecting "Option 2." Anyone who believes he has undergone an unfavorable reaction on health following the use of the product is invited to call his doctor immediately.

Unfortunately, it is not the only medicinal reminder that has been published recently. On March 27, the FDA announced that Amneaux pharmaceuticals had drawn four lots from his Vancomycin hydrochloride For an oral solution, USP, 250 mg / 5 ml of market antibiotics.

Drugs are generally used to treat "enterocolitis caused by Staphylococcus aureus (including strains resistant to methicillin) and pseudomembrane colitis associated with antibiotics caused by It's hard . "A manufacturing error has led to certain over-reproductive packages and exceed the maximum daily dose of 2 grams, which could cause potentially serious side effects.