logo
Welcome Guest! To enable all features please Log ind or Registrering.

Notifikation

Icon
Error

pysong
#1 Skrevet : 31. juli 2023 05:07:09(UTC)
pysong

Rang: Advanced Member

Gruppe: Registered
Tilmeldt: 01-02-2023(UTC)
Indlæg: 628

Male enhancement pill recalled for containing undisclosed prescription drugs



A dietary supplement is being recalled because it is tainted with the active ingredient in the prescription drugs Viagra and Cialis.To get more news about vigrx oil prices, you can visit vigrxplus-original.com official website.

The Food and Drug Administration says the recall involves one lot of Volt Candy’s PrimeZen Black 6000. The recall was initiated after an FDA analysis found the product was tainted with sildenafil and tadalafil.
Sildenafil and tadalafil are the active drug ingredients found in Viagra and Cialis, respectively. They are restricted to use under the supervision of licensed healthcare professionals. The FDA said these undeclared ingredients may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels.

The recall comes as the FDA is warning companies that selling products that contain undisclosed or hidden prescription medication violates federal law. In early July, the FDA sent warning letters to four companies that sold honey products that contained undeclared active ingredients, including sildenafil and tadalafil.
Because the product is listed as a dietary supplement, it is regulated by the FDA as food, not drugs. Under the law, the FDA does not have the authority to approve dietary supplements for safety and effectiveness or approve their labeling. It is the company’s responsibility to make sure its products meet safety standards and are not violating the law.

However, tadalafil and sildenafil products are excluded from the dietary supplement definition. Their presence makes the products unapproved drugs for which safety and efficacy have not been established.

Anyone who experiences a side effect or bad reaction should report it to their health care professional and FDA, which has said even a single adverse event report can help them identify a potentially dangerous product and possibly remove it from the market.
Brugere som besøger dette emne nu:
Guest
Hop til Forum  
Du kan ikke skrive nye indlæg i dette forum.
Du kan ikke svare på indlæg i dette forum.
Du kan ikke slette dine indlæg i dette forum.
Du kan ikke ændre dine indlæg i dette forum.
Du kan ikke lave afstemninger i dette forum.
Du kan ikke stemme i dette forum.