Propecia® Attorneys Jacksonville FDA Recall, Warning or Action: The FDA has listed finasteride (the active ingredient of Propecia®) as a Pregnancy Category X drug. NOTE: Pregnant women should never handle this drug because it is known to cause serious birth defects. Several medications have been cleared from pharmacy shelves after cases of serious side effects are reported to the Federal Drug Administration. We relentlessly track the rulings handed down by the state and federal courts for claims related to defective medications and failed healthcare device companies. In some incidences, the manufacturer, distributor or FDA will have taken steps to recall the dangerous drug and/or furnish improved instructions or warnings. Side Effects of Propecia® Use Propecia® (finasteride) is classified as a synthetic 5 alphareductase inhibitor. This drug is designed to treat male pattern baldness by targeting enzymes that convert testosterone into DHT which stops further balding. This drug also treats benign enlargement of the prostate. Possible serious side effects or negative patient outcomes include: Erectile Dysfunction Testicular Pain Lumps and Pain in the Breast Prostate Cancer Male Breast Cancer Birth Defects if Handled by Pregnant Women NOTE: Propecia® is meant for men and should never be used by women or children. Men who take Propecia® are urged not to donate blood and the drug can stay in the blood stream for a month after the last dose. Our accident injury lawyers can provide the best legal information regarding your case and help you determine if you have a valid lawsuit. If you or a loved one was injured due to a defective drug or failed medical device, defending your rights can be an uphill battle. Contact a liability 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.