Zoloft® Attorneys Jacksonville

FDA Recall, Warning or Action: The U.S. Food and Drug Administration has repeatedly warned consumers with new alerts about the consequences and serious complications of taking antidepressant drugs like Zoloft®.

Several prescription anti-depressant drugs have been required to include package warnings of potentially serious side effects. We relentlessly monitor the outcomes handed down by state and federal courts for cases involving dangerous products and negligent drug manufacturing companies. In some cases the fault comes from the pharmaceutical company’s failure to identify contraindicated situations and accurately list known side effects or negative outcomes.

Side Effects of Zoloft® Use

Zoloft® has become one of the most widely prescribed antidepressants available in the United States. In recent years, however, the prescription drug has been linked to dangerous conditions. Among the most devastating are the following birth defects:

  • Atrial Septal Defects
  • Ventricular Septal Defects
  • Persistent Pulmonary Hypertension
  • Spina Bifida
  • Congenital Heart Defects
  • Abdominal Defects (Omphalocele)
  • Craniosynotostosis (Skull Defects)
  • Tetralogy of Fallot with Pulmonary Atresia

NOTE: During the 1990s, concerns emerged that the drug led to increased thoughts of suicide and violent behavior. The drug’s manufacturer, Pfizer, faced numerous lawsuits over increased suicide risks.

Though money cannot bring back your wellness or return a family member, it can help to pay the bills. If you or a loved one has been injured by or permanently damaged due the failure of a manufacturer or seller to exercise reasonable care by providing a safe product, contact a personal injury lawyer at 904-251-1111 or 1-800-251-1111; or use this website’s Do I Have A Case form for a prompt response.

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