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In 2004, the FDA and GlaxoSmithKline alerted healthcare professionals about the dangers of Paxil controlled-release tablets. This FDA alert came in response to mounting evidence that anti depressants may cause suicidal thoughts in children and adolescents. The Food and Drug Administration is currently studying the frequency of these side effects in adults.
The Food and Drug Administration releases alerts when the public may be at risk if they take a specific drug that has been linked to health problems. FDA alerts are taken very seriously by pharmaceutical companies and the medical community. Patients have a right to be aware of the risks associated with any medication they are taking. The fact that FDA alerts exist on anti depressant drugs is an indication of the dangerous side effects users of these medications may be exposed to.
If your life has been affected by FDA alerts on antidepressant drugs, you deserve to be aware of the risks of these prescription medications. An experienced attorney can help you take legal action against those who are responsible for your pain. Do not hesitate to discuss your case with an understanding lawyer today.
