TDF Attorneys in Sacramento

if you've been harmed by a TDF drug, call (916) 520-6639 now!

What is TDF?

Tenofovir disporxil fumarate (TDF) is an antiviral drug that is commonly prescribed to improve the quality and length of life for people with HIV. However, it has been reported that the drug causes kidney disease and bone injuries.

TDF contains the active ingredient tenofovir, which stops HIV from multiplying. But clinical studies and FDA monitoring revealed the specific composition and use of TDF drugs is associated with the gradual loss of kidney function and diminished bone mineral density.

  • Gilead Sciences has five TDF drugs on the market:
  • Viread
  • Truvada
  • Atripla
  • Complera
  • Stribild

Current lawsuits against Gilead allege the company purposefully withheld safer versions of its antiviral drug and deceptively marketed the TDF based drugs as “miracle drugs” with no or minimal toxicities.

Negligence of Drug Manufacturer Gilead sciences

Gilead first developed and released Viread, an HIV treatment drug, in 2001. That same year, Gilead began to develop tenofovir alafenamide fumarate (“TAF”) to try to minimize the adverse effects of TDF.

John Milligan, Gilead’s former President and Chief Executive Officer, called TAF the “kinder, gentler version of Viread” because it can be given at a dramatically lower dose than TDF while being just as effective.

In developing its subsequent antiviral drugs, Gilead had a choice to use TDF or to use TAF, the safer design for delivering the active ingredient tenofovir into the body. For nearly 15 years, Gilead chose to continue to use TDF despite its known adverse effects in patients. Milligan later admitted that the real reason Gilead withheld the safer TAF design was because they did not want to hurt TDF sales by admitting that TDF was not the “miracle drug” Gilead claimed it was.

If you or your loved one has taken a TDF drug and suffered adverse side-effects, call our firm today at (916) 520-6639 to discuss your case in a free consultation!

FDA Cracks Down on Gilead

The Food and Drug Administration (FDA) has twice reprimanded Gilead for unlawfully minimizing the risks of TDF.

  • Gilead continues to downplay the risks of TDF by:
  • Misrepresenting the drugs as safe
  • Dismissing TDF associated adverse events as purportedly unavoidable side effects of tenofovir
  • Discouraging doctors from monitoring patients by using more sensitive markers of kidney function

Moreover, Gilead’s misleading statements to doctors have further undermined the inadequate warnings of TDF adverse effects in drug labels. Current lawsuits allege that if Gilead had given adequate warnings and monitoring instructions, doctors would have heeded them and detected TDF toxicity earlier through better, more frequent monitoring, and thereby preventing or lessening patients’ injuries.

What Are the Dangers of TDF?

People taking any TDF drug should be advised of its serious health risks. In recent clinical studies, researchers have found higher rates of declining kidney function and reduced bone mineral density in patients after 1 -2 years use of TDF, and in as few as 3 months of TDF use.

Common symptoms of kidney disease include:

  • Loss of appetite
  • Fatigue
  • Poor concentration
  • Swelling of feet and ankles
  • Itchy skin
  • The need to urinate frequently
  • High blood pressure

Common symptoms for declining bone mineral density include:

  • Back pain
  • Stooped posture
  • Loss of height
  • Bone fractures from minor stress or falls

Other TDF side effects allegedly include liver problems and lactic acidosis, a condition that causes lactic acid to build up in the body, resulting in low pH levels.

Do I qualify for a TDF Lawsuit?

Kershaw, Cook & Talley is currently handling TDF injury cases in California and nationwide. If you've taken a TDF drug and suffered adverse side-effects, you may qualify.

You have taken any of the following medications to treat or prevent HIV:

  • Viread
  • Truvada
  • Atripla
  • Stribild
  • Complera

You have suffered any of the following injuries after consistent usage of a TDF drug:

  • Chronic Kidney Disease
  • Acute kidney injury
  • Severe renal deficiency
  • Fatal renal insufficiency
  • End-stage renal disease
  • Loss of bone density
  • Low bone mineral density
  • Bone loss
  • Bone breaks or fractures
  • Bone necrosis
  • Tooth loss attributed to bone density disorder
  • Fanconi Syndrome
  • Osteomalacia (before the client turns 55 yrs old)
  • Osteoporosis w/pathological fracture

Further criteria include:

  • No history of extended use of hard drugs (heroin, crack, meth) within the time of taking TDF and diagnosed with kidney disease or bone density loss
  • No prior legal representation
  • No longer taking TDF drugs (Viread, Truvada, Atripla, Stribild, or Complera)
  • No diabetes
  • No prior or current chemotherapy
  • No diagnosed eating disorders
  • Generally compliant with prior or current HIV medication
  • Residents of Tennesee, Kentucky, and Louisiana

Consult with Our Skilled Legal Team Today

If you want to gain a more comprehensive understanding of the merits of a potential claim against Gilead Sciences, you should seek advice from one of our experienced TDF lawyers at Kershaw, Cook & Talley. Our legal team boasts more than a century’s worth of collective legal experience litigating personal injury matters, including issues involving dangerous products like TDF antiviral drugs. With us, you can expect to have a devoted advocate who can skillfully read the legal landscape to help you find an effective path to secure the justice you deserve.

Call us at (916) 520-6639 to learn more about how our law firm can assist you. Schedule your free initial consultation today.

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  • Sorry, you must have used at least one of the following treatments.
  • When (date) were you prescribed the medication(s)?
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