The U.S. Food & Drug Administration (FDA) has issued a warning for consumers not to take SARMs like LGD-3303, as the unapproved bodybuilding supplements have been found to contain illegal adulterated drugs which may increase the risk of serious side effects.
Free Confidential Lawsuit Evaluation: If you or a loved one has been injured by the side effects of LGD-3303 or another SARM, you should contact our law firm immediately. You may be entitled to compensation by filing a suit against the manufacturer and our lawyers can help.
What are SARMs?
Selective androgen receptor modulators, or SARMs, are unapproved and under-researched drugs purported to boost a user’s athletic performance and make them appear more muscular by mimicking the effects of testosterone without the negative side effects of traditional steroids.
The standard starting dose of LGD-3303 is approximately 1 mg/kg/day.
SARMs Side Effects
- Liver damage
- Cardiovascular complications
- Heart attack
- Blood clots
- Deep Vein Thrombosis (DVT)
- Pulmonary Embolism (PE)
SARMs Contain Unapproved Substances: JAMA Study
A study published in the Journal of the American Medical Association (JAMA) in Nov. 2017 found that many SARM products contain unapproved substances, hormones, and steroids. The researchers also found that some of these drugs have incorrect and/or misleading labeling.
For the study, the researchers analyzed 44 drugs marketed as SARMS using procedures approved by the World Anti-Doping Agency (WADA) for detecting banned substances in athletes. They found that 39% of the supplements contained unapproved drugs, like banned growth hormones or steroids, while 25% contained similar substances not even included on the label. In 59% of the products tested, the amount of compounds listed on the label was significantly different than what the analysis actually found.
Can I File a SARMs Lawsuit?
Only a qualified attorney can determine whether you are eligible to file a lawsuit against the maker of LGD-3303, which is why we are currently offering free case evaluations. Simply fill out the confidential evaluation form below to contact our law firm now.
Most cases involving pharmaceuticals allege that a drug was sold with design, manufacturing, and/or marketing defects, which typically refers to a company’s failure to warn of a certain side effect. In the case of LGD-3303, our attorneys suspect that patients may be able to take legal action in light of claims that the manufacturer failed to adequately warn doctors and patients about the risk of severe liver damage and cardiovascular complications.
- LGD-3303 (GW-501516)
- Ostarine MK-2866
- ”The Lieutenant”
- “The Officer”
- GSX-007 or S-4
- And more
Do I have a LGD-3303 Lawsuit?
The Pharmaceutical Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in SARMs lawsuits. We are handling individual litigation nationwide and currently accepting new liver damage and cardiovascular complications cases in all 50 states.
Free Case Evaluation: Again, if you had a heart attack, stroke, blood clot, or other serious health problem after taking SARMs, you should contact our law firm immediately. You may be entitled to compensation by filing a suit and we can help.