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34 Propecia Studies Inadequately Reported Sexual Problems

34 Propecia Studies Inadequately Reported Sexual Problems

April 6, 2015 — Out of 34 clinical trials of Propecia, none adequately reported sexual side effects, according to an analysis published in JAMA Dermatology.

Propecia (finasteride) works by making massive changes to hormone levels in a man’s body, which can have unintended side effects on sexual function. It prevents the conversion of testosterone into more-potent 5α-dihydrotestosterone (5α- DHT), which reduces 5α- DHT levels by 70%.

None of the studies provided enough information about the severity, reversibility, or frequency of sexual side effects. Side effect reporting was “partially adequate” in 19 studies (56%), inadequate in 23 studies (35%), and 3 studies (9%) reported no adverse events.

Dr. Steven Belknap, lead author of the analysis, warned that there is insufficient information to assume Propecia is safe:

“Was this information obtained but then not included in published articles? Or, were these clinical trials performed in a way that simply didn’t capture this essential information? And most importantly, is the risk to benefit ratio of finasteride acceptable?”

In recent years, there has been growing concerns about long-term sexual dysfunction from Propecia. The FDA has already issued warnings about sexual side effects, including erectile dysfunction, low libido, ejaculation disorders, and orgasm disorders that continue after Propecia is discontinued.

Merck & Co. is now facing hundreds of lawsuits from men who allege they were not adequately warned about the risk of long-term sexual dysfunction.

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The Schmidt Firm, PLLC is currently accepting Propecia induced injury cases in all 50 states. If you or somebody you know was diagnosed with sexual dysfunction, you should contact our lawyers immediately for a free case consultation. Please use the form below to contact our Defective Drug Litigation Group or call toll free 24 hours a day at (866) 920-0753.

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