Good Lifestyle

You know almost what to expect when you head for the pharmacy, whether it is a prescription or an over -the -counter relief (OTC). But what youdon't expect drugs that arepart of a major reminder, potentially you or your loved ones in danger. Unfortunately, this is exactly what happened with a popular variety of drugs sold at CVS, Rite Aid and Walgreens, among other pharmacies. Read the rest to find out which drugs are now subject to a widen recall and why the Food and Drug Administration of the United States (FDA) says that you should not take them.

Read this then:If you take this painting against pain, stop now, the FDA warns.

Reminders are more common than you think, and the FDA and the Consumer Product Safety Commission in the United States (CPSC) work to issue warnings and keep the public aware. On June 29, the FDA announced that Bryant Ranch Prepack Inc. had published a voluntary reminder ofMorphine sulfate 30 mg extended release tablets and morphine sulphate 60 mg extended liberation tablets due to a mixture of labels.

The CPSC also published three different recall announcements on June 16 for acetaminophen, which is more commonly known with the Tylenol brand name, due to a lack ofChildren's resistant packaging. Two acetaminophen varieties of the Kroger brand, manufactured bySun pharmaceutical industries and Auohealth,were affected, just like aWalgreens store brand Acetaminophen, also manufactured by Aurohealth.AE0FCC31AE342FD3A1346EBB1F342FCB

Now the FDA has published a reminder ad for a drug that has already led to three serious side effects.

On July 25, Smyrna, based in Smyrna, in Tennessee, Vi-Jon, LLC announced an expansion of its voluntary recall asLAXATIVE SALINE SALINE CITRATE Magnesium solution Include 63 additional products "in the expiration of the consumption level".

The recall now includes all flavors and a lot of drugs, namely cherry flavor and grape flavor, wrapped in ounce bottles with 10 fluid. The initial recall waslimited to a lot CVS Magnesium Citrate Saline LAXATIVE Oral solution lemon solution, according to the original announcement of June 21, which was then extended on July 14Include all lots From lemon product sold to other retailers.

According to the announcement of July 25, vine, lemon and cherry products were available for purchase in Rite Aid, Walgreens and CVS stores on a national scale, as well as grocery stores such as Walmart, Publix, Kroger And Harris Teeter, among others. The products were also distributed at wholesale points of sale, and VI-Jon said that the company "continues its investigation into the cause of the problem".

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The laxative product is taken "to relieve constipation (irregularity)", generally leading to a saddle within 30 minutes to six hours, said the announcement of recall. But the products are now recalled after third -party microbial tests have foundLiquefaciens gluconacetobacterbacteria.

To date, VI-Jon has received three serious unwanted reactions reports which could be linked to the recall, after having increased a report noted during the announcement of July 14.

The bacteria itself has been described as a "vegetable pathogen", according to a2020 Case study a patient with advanced liver cirrhosis also infected with "Gluconacetobacterspecies. "According to the case report, there was only another case of human infection which was" associated with severe immunodeficiency ".

The FDA notes that immunocompromised patients should be wary of recalled drugs because they "can be at increased risks of invasive infections caused byLiquefaciens glucanacetobacter This could lead to serious and potentially fatal unfavorable consequences. ""

If you have bought these laxatives, you can be contacted by Vi-Jon by e-mail or by phone, and the company will then provide information on how to return or destroy the product. But take you on you to check your pharmacy cabinet immediately, because the FDA asks consumers to stop using recalled products and returning any product remaining at your place of purchase.

If you have experienced harmful effects in relation to this product, the FDA asks you to contact your doctor or health care provider. For questions related to the recall, you can send an email to vi-jon at a [email protected] from Monday to Friday between 7:30 a.m. and 4:30 p.m. Central time.