FDA Warning For Propecia Erectile Dysfunction (ED) Side Effects

The long-term side effects from Propecia (generic name Finasteride) will likely mean the FDA orders the manufacturer of Propecia, Merck & Co., Inc., to significantly strengthen the drug's warning. As of May 7, 2011, Merck's products contain no warning that the use of Propecia or Proscar can cause permanent erectile dysfunction (ED), impotence, and loss of sex drive.

Propecia Lawsuits for Failure to Adequately Warn of Erectile Dysfunction (ED) Side Effects

Men who used Propecia were not warned that they could develop permanent erectile dysfunction (ED) and other side effects from using Propecia. Manufacturers of prescription drugs have a duty to warn users of the potential side effects their drugs cause. If a man has developed permanent erectile dysfunction, impotence, or loss of libido after using Propecia before the FDA warning, he may have a legal claim against the drug manufacturer for failure to warn. A Propecia lawsuit obviously is not a cure, but it is the only avenue for seeking redress for the wrong done by the drug's manufacturer for not warning men of the side effects.

DeCarli Law's Propecia Lawyers Offer Free, Confidential Consultations for Propecia Side Effect Injuries

The side effects caused by Propecia are embarrassing, which is why the Propecia Attorneys at DeCarli Law offer confidential consultations for men injured by Propecia, Proscar or Finasteride. Our telephone consultations are free, and you will speak to an actual attorney, not a legal assistant or staff person. If you have been injured by Propecia, please consider filling out the confidential contact form to the left to schedule a consultation to learn more about your legal rights.

Report Your Propecia Side Effects to the FDA

If you believe Propecia has caused you to develop erectile dysfunction (ED), impotence, loss of libido, or any other decreased sexual function, please report your side effects to the FDA. You may do so by clicking on the logo to the left. Informing the FDA of your injury helps the agency understand the scope of the problem.

The information on this website is for general information purposes only. Nothing on this or associated pages, documents, comments, answers, emails, or other communications should be taken as legal advice for any individual case or situation. The information on this website is not intended to create, and receipt or viewing of this information does not constitute, an attorney-client relationship. DeCarli Law only represents individuals pursuant to a signed, written contract.

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Debra DeCarli and Bob DeCarli are licensed by the State Bar of Texas and the State Bar of California.

DeCarli Law represents drug side effects and defective medical devices personal injury clients for claims, lawsuits and settlements in Alabama AL, Alaska AK, Arizona AZ, Arkansas AR, California CA, Colorado CO, Connecticut CT, Delaware DE, Georgia GA, Hawaii HI, Idaho ID, Illinois IL, Kansas KS, Maine ME, Maryland MD, Massachusetts MS, Minnesota MN, Mississippi MS, Montana MT, Nebraska NE, New Hampshire NH, New Jersey NJ, New Mexico NM, New York NY, North Carolina NC, North Dakota ND, Oklahoma OK, Oregon OR, Rhode Island RI, South Carolina SC, South Dakota SD, Tennessee TN, Utah UT, Vermont VT, Virginia VA, Washington WA, Washington D.C, West Virginia WV, Wisconsin WI and Wyoming WY. The attorneys of DeCarli Law are licensed in California and Texas. DeCarli Law's practice includes lawsuits for Propecia side effects, Finasteride lawsuits, Topamax lawsuits, Fosamax lawsuits, Gadolinium lawsuits, NSF lawsuits, Nephrogenic Systemic Fibrosis Lawsuits, YAZ lawsuits, Yasmin lawsuits, Ocella lawsuits, and Zarah lawsuits.