Truvada Lawsuit

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The attorneys of Nadrich and Cohen are currently investigating Truvada Medication Side Effect claims. Gilead Sciences Inc. is facing a lawsuit with over 40 plaintiffs over accusations that it knowingly sold a dangerous HIV medication and intentionally withheld a newer, safer HIV medication from the market in order to profit from the older medication’s patent for a longer time period. The lawsuit alleges that Gilead sold HIV medications, like Truvada, containing tenofovir disoproxil fumarate (TDF) despite knowing since 2001 that it was “highly toxic in the doses prescribed and risked permanent and possibly fatal damage to the kidneys and bones.” TDF was used in the following Gilead HIV medications:

  • Truvada
  • Stribild
  • Viread
  • Complera
  • Atripla

If you or a loved one were diagnosed with kidney disease and/or bone density loss after taking Truvada or one of the above HIV medications you may be eligible for financial compensation. Call 1-800-718-4658 today for a free, confidential case evaluation, use the live chat, or fill out the free, confidential “Do I Have A Case?” form on this page.

Why Are Truvada Patients Suing Gilead?

The accusation that Gilead knowingly sold a dangerous medication to HIV patients is shocking. However, equally shocking is the accusation that Gilead intentionally withheld its newer, safer HIV medication Tenofovir Alafenamide (TAF) from the market in order to maximize its profits.

The lawsuit alleges that Gilead knew that TAF was much safer than TDF as far back as 2002, yet chose to not release this research or bring TAF to the market until 2015, when Gilead’s patents on TDF expired. This allowed Gilead to profit from a longer period of FDA exclusivity regarding TDF.

The lawsuit claims that Gilead intentionally made sure that its patient and prescriber labeling did not contain adequate warnings that TDF patients need to be regularly monitored for signs of kidney and bone damage. The lawsuit says Gilead did this for the purposes of hiding TDF’s true risks and maximizing its own profits.

Gilead also raised the cost of some of its TDF-based drugs right before TDF’s  patent expired. This was a clear attempt to get consumers to switch to its TAF-based medications before generic versions of TDF hit the market.

PrEP

Truvada Side Effects

Patients who have taken Truvada or other HIV PrEP drugs may be eligible for financial compensation if they have been diagnosed with one of the following injuries or conditions while using a TDF medication :

  • Osteopenia
  • Osteoporosis
  • Bone Fracture
  • Chronic Kidney Disease
  • Renal Tubular Dysfunction
  • Worsening Kidney Function
  • Acute Kidney Injury
  • Acute Renal Failure
  • Fanconi Syndrome

We believe that over 25,000 HIV patients  may have been diagnosed with a serious side effect after taking TDF. These side effects include bone density loss and kidney disease. TDF use has also been found to increase the risk of bone fractures by 40 percent and nearly 6,000 bone fractures have so far been linked to TDF use.

Truvada Bone Side Effects

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Patients have reported being diagnosed with Osteopenia, Osteoporosis and bone fractures while using Truvada and other TDF-containing HIV medications.

One patient reportedly took TDF for 11 years and was diagnosed with osteoporosis and osteopenia of the hip, neck and spine at the age of 35.

A 58-year-old patient who took TDF says his doctor told him that the severe demineralization which took place in his bones left him with the bones of an 85 year-old woman. A 2016 study showed that TDF use was associated with a 1-3% increase in bone mineral density loss compared to the loss associated with “other agents.”

Truvada Kidney Disease Side Effect

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Patients have reported being diagnosed with acute kidney injury, worsening kidney function, acute renal failure, Fanconi Syndrome and chronic kidney disease while taking Truvada and other TDF medications.

Studies have also associated TDF use with 2.25 times the risk of developing chronic kidney disease when compared to other drugs, as well as a 33% increase in the risk of developing chronic kidney disease for each year the drug is taken.

One patient, reportedly took TDF for 10 years and, at age 59, was diagnosed with Fanconi Syndrome, a rare kidney disease

Top Drug Side Effects Attorneys

You deserve to have the best representation if you’ve suffered kidney disease and/or bone density loss after taking Truvada or HIV PrEP meds. Nadrich & Cohen, LLP are the experts in products liability and dangerous drug side effect claims. Our drug side effect attorneys and legal teams have a proven track record or getting maximum compensation for drug side effect victims and their families.

Why Choose Nadrich & Cohen?

Your case will be in capable hands with the strong, battle-tested lawyers at Nadrich & Cohen, who have over 70 years of combined legal experience and have obtained over $350,000,000 on behalf of clients since the firm’s founding in 1990.

Our founding principle is “the client always comes first,” and we show this by only representing plaintiffs and limiting our employees workloads so they can devote personal, individual attention to every single one of our clients.

Your questions will always be answered by our compassionate, polite and professional staff, who will always promptly respond to your calls and emails.

Request A Free Consultation Now

You may be entitled to a financial recovery if you or a loved one has been diagnosed with kidney disease and/or bone density loss after taking Truvada, Stribild, Viread, Complera and Atripla. Call us today at 1-800-718-4658 for a confidential, free consultation. Don’t wait as there are strict time limits for making a claim.

We handle claims nationwide.