Crime & Safety

Pharm Company Put Profits Over Patients, AG Says: RI Will Collect $235,269 In Abilify Settlement

Atty. Gen Peter Kilmartin announced Rhode Island and 18 other states settled a lawsuit against pharmaceutical giant Bristol Myers Squibb.

PROVIDENCE, RI – Attorney General Peter F. Kilmartin announced today that he, along with 42 other attorneys general, reached a $19.5 million dollar settlement with Bristol-Myers Squibb Company. The Attorneys General alleged the company's marketing of Abilify violated the deceptive trade practices Act.

Rhode Island will receive $235,269 through this settlement

Abilify is the brand name for the prescription drug aripiprazole, which is described as an atypical antipsychotic drug. The U.S. Food and Drug Administration originally approved it in 2002 for the treatment of schizophrenia.

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Since then, the FDA has approved various formulations of Abilify for several indications. This complaint, however, alleges that BMS promoted Abilify "for use in elderly patients with symptoms consistent with dementia and Alzheimer’s disease despite the lack of FDA approval for these uses and without first establishing the drug’s safety and efficacy for those uses."

According to the press release, the company was warned about problems.

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"In 2006, Abilify received a “black box” warning stating that elderly patients with dementia-related psychosis who are treated with antipsychotic drugs have an increased risk of death. Additionally, the complaint alleges that BMS promoted Abilify for uses in children not approved by the FDA. Moreover, the complaint alleges that BMS minimized and misrepresented risks thereby making false and misleading representations about Abilify’s risks.

"The complaint further alleges that BMS also overstated the findings of scientific studies by not revealing limitations that would materially affect the interpretation of the study results. The active ingredient in Abilify, aripiprazole, is now available as a generic, but several product formulations are still protected by patent.

“Bristol-Myers Squibb purposefully did an end run around the FDA approval process in order to enhance profits, while putting vulnerable patients at risk,” said Kilmartin. “This isn’t the first time a pharmaceutical company has put profits ahead of patients, which is why our partnership with attorneys general across the country to investigate this deceptive practice is critical to keeping these companies honest.”

"The terms of the settlement restrict BMS’ marketing of any formulation containing the active ingredient aripiprazole. BMS will be prohibited from making false or misleading claims about Abilify, about its safety or efficacy in comparison with other drugs, and about the implications of clinical studies relating to the drug. BMS will also be subject to limitations on financial incentives to sales representatives and health care providers, dissemination of information that may promote off-label use of Abilify, and other practices affecting off-label promotion.

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