Johnson & Johnson settled the seventh Risperdal case scheduled to go before a jury in Philadelphia’s mass tort program on January 6, just three days before the trial was to begin.
The latest lawsuit involved a New York man who alleged that he developed gynecomastia as a result of taking the antipsychotic medication Risperdal.
The plaintiff was prescribed the drug “off-label,” meaning for a use that was not approved by the U.S. Food and Drug Administration (FDA), and took it from 2002 until 2011.
The FDA did not approve Risperdal for use in children and adolescents until 2006.
Gynecomastia is a condition in which boys and men develop tender and swollen breasts.
Surgery is often required to correct the condition, although liposuction can be effective in removing excess breast tissue in mild to moderate cases.
In more severe cases, patients may need a mastectomy to remove breast tissue and excess breast skin.
A 2014 study presented at an annual meeting of the American Association for Geriatric Psychiatry concluded that users of Risperdal might face as much as a 69 percent increased risk of gynecomastia compared to those who have not taken the medication.
Because of the study’s results, researchers suggested that doctors prescribe Zyprexa or Seroquel to males instead of Risperdal to reduce the chances of developing gynecomastia and other harmful conditions and side effects.
Johnson and Johnson has maintained a busy litigation schedule related to its antipsychotic medication for over a year:
Two more Risperdal cases are scheduled for trial on February 21, according to the Philadelphia Court of Common Pleas Trial Division.
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Camp Lejeune’s water contamination issue spanned several decades starting in the 1950s. Exposure to these chemicals has been linked to various serious health issues, including cancer, organ diseases, and death.
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Here, at TruLaw, we’re committed to helping victims get the justice they deserve.
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