FDA Didn’t Learn from SSRI Antidepressant Birth Defect Lawsuits

The federal Food and Drug Administration is not yet a target of claims by Prozac birth defect class action lawsuit attorneys. That doesn’t mean that they don’t use the agency and its lack of pressure on manufacturers like Eli Lilly and Co. to make their arguments. Perhaps that may have played a role in how the FDA is looking at antidepressant birth defect side effects.

Or maybe not. In yet another questionable plan, it was only two weeks ago that the agency created a database and doctor training program for immunosuppressive drugs that cause similar birth defect side effects. While Zoloft birth defect side effects can be devastating, one-in-five organ transplant patients who exposed their fetuses to the drugs saw birth defects.

The agency works hand-in-hand with the National Institutes of Health. Yet like the complaints of Prozac birth defects lawsuit lawyers, it could be argued that the FDA delayed the updated warnings and pregnancy registry for too long. After all, the NIH noted the elevated risk for birth defect side effects in drugs like CellCept and Myfortic some three years ago.

If you or someone you know has been affected by SSRI antidepressant birth defect side effects, you’re not alone. Visit the Zoloft, Paxil, Celexa, Lexapro & Prozac SSRI Antidepressant Birth Defect Class Action Lawsuit Investigation to learn more about what legal options you have. Fill out the short from, and a qualified Prozac birth defects lawsuit lawyer will contact you for a free review of your potential case. Lives may be irrevocably affected by these antidepressant pregnancy side effects, but you may be able to get financial assistance. Get your no-cost legal consultation today.