Why is oxyelite pro unavailable

The supplement OxyElite Pro is a common link in 24 cases of non-viral hepatitis in Hawaii and appears to now contain a substance that has not been safety tested for human consumption, according to the U. Food and Drug Administration. Two of the patients required liver transplants, and a third patient died. OxyElite Pro and a variety of other fitness supplements that had contained the stimulant DMAA were pulled from military shelves following the collapse and death of three soldiers during training at Fort Bliss, Texas, two years ago.

A Department of Defense safety review, completed in June, found the ingredient DMAA increased the risk of serious injury for tens of thousands of servicemembers who used the supplements while working out. There was no other dietary supplement or medication use reported in common by more than two patients. National case finding efforts have included surveillance of poison center data using the National Poison Data System.

A call for cases was also disseminated through the United Network for Organ Sharing listserv to transplant programs across the country. These activities have identified four persons in states outside of Hawaii with reported OxyELITE Pro or other weight loss or muscle-building dietary supplement use prior to the development of acute hepatitis of unknown cause. One of these is a resident of Hawaii who obtained their product in Hawaii but was diagnosed in a different state. CDC, in collaboration with state health departments, is collecting additional clinical and epidemiologic information from these persons to determine if this outbreak is nationwide.

Results from FDA product testing are pending. While the investigation is ongoing and these data are preliminary, clinical data, laboratory tests, and histopathology of liver biopsy specimens collected thus far suggest drug- or herb-induced hepatotoxicity. Drug- and herb-induced hepatotoxicity have been reported in association with exposure to a variety of drugs and herbs used as dietary supplements and can lead to severe acute hepatitis and liver failure 1,2.

Drug- and herb-induced hepatotoxicity often resolves following discontinuation of the product 3. Attributing liver injury to a specific ingredient can be challenging because of multiple ingredients, product variability, and lack of testing to confirm exposure to a product. Clinicians evaluating patients with acute hepatitis should ask about consumption of dietary supplements as part of a comprehensive evaluation.

Clinicians should report patients meeting the case definition to the local or state health department, as well as the FDA's MedWatch program. Clinicians can discuss patient management options with a medical or clinical toxicologist by calling their local poison center at Persons who use dietary supplements for weight loss or muscle gain should do so with caution and under a medical provider's close supervision.

Before I go any further, allow me to note that I am not a lawyer, nor is any employee of mine. We are not affiliated with USPLabs in any way, shape, or form. This site does not physically sell any products, nor do we warehouse or distribute them. But that does not make a law. That does not make a fact. And the fact is, the stimulant has never been proven to be the stimulant that has caused anybody health problems when used properly per the label. That is the truth. The process went something like this:.

USPLabs claims the stimulant is a natural constituent of geranium Pelargonium graveolens. Depends on who you ask and where they get it from…. But was Eli Lilly using it as a supplement? Maybe not, but geranium oil was. And again, we come to the question of the burden of proof.

The products contain 1,3 Dimethylamylamine HCL, and their labels state it as such.