LOS ANGELES--(BUSINESS WIRE)--Apr 11, 2019--41 patients from 12 states nationwide who are living with HIV or AIDS or were on PrEP filed a personal injury lawsuit against The lawsuit was filed by 41 individuals who suffered bone and/or kidney damage as a result of taking Gilead’s TDF despite the fact that the company knew as far back as 2001 that it was Plaintiffs in today’s case against Gilead hail from TDF is prescribed and sold by Gilead under the brand name As such, thousands and thousands of HIV/AIDS patients may have been unwittingly exposed to significant kidney and bone damage from TDF as a component of their ostensibly lifesaving antiretroviral drug regimens—all manufactured and sold by Gilead. “I contracted HIV through my work as a nurse serving others and then learned that my kidneys and bones were damaged from taking Gilead’s TDF based drugs for HIV. INDUSTRY KEYWORD: HEALTH AIDS INFECTIOUS DISEASES PUBLIC POLICY/GOVERNMENT PHARMACEUTICAL OTHER POLICY ISSUES PROFESSIONAL SERVICES LEGAL This gross profiteering explains why less than half of people living with HIV in the U.S. are virally suppressed, one of the lowest rates among the world's high-income countries,” Goodrow, one of the plaintiffs, said in a statement through the legal firm Hilliard & Shadowen, LLP.Jason Walker, another plaintiff, said the “no-generics restraints crafted by Gilead and its co-conspirators” are detrimental to innovation in HIV treatment.
Since those initial filings, HIV Litigation Attorneys™ have continued the fight against Gilead with other lawsuits filed in the federal courts. In addition, many HIV-negative individuals seeking to prevent HIV acquisition may have suffered similar harm to their kidneys or bones from taking Truvada as part of their PrEP protocol.Today’s case filing asserts that Gilead’s zeal to maintain and maximize its corporate profits came at the expense of the health and wellbeing of its customers who were prescribed and taking TDF.
The plaintiffs noted that a generic version of Complera, combined with Janssen’s still-on-patent rilpivirine would sell for no more than half that amount. We look forward to working with this new group of plaintiffs from around the country to hold Gilead accountable and seek justice for the people it has harmed.
I am glad that my voice and the voices of others who have been taken advantage of for more profits will finally be heard,” said “More and more plaintiffs are coming forward to tell their stories of how they have been harmed by Gilead’s practice of putting profits over patient health.
Additionally, the plaintiffs argued that the prices of more than 50 percent of core agents, such as protease inhibitors, integrase inhibitors and 75% of booster drugs are also artificially inflated due to these agreements. The second was a class action lawsuit against Gilead on behalf of all HIV-positive individuals who purchased TDF drugs and suffered similar health problems as a result of long-term exposure to TDF drugs. http://www.businesswire.com/news/home/20190411005808/enPress release content from Business Wire. Teva Pharmaceuticals is expected to begin marketing its Truvada generic next year.© 1985 - 2020 BioSpace.com. The plaintiffs have argued that agreements between the two companies prohibit Janssen from making that generic-containing version of the drug or from licensing rilpivirine to generic manufacturers that would make it.The companies, the plaintiffs argue, have a “no-generics” policy, which keeps the price of the drugs high.
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