Unregulated male sexual enhancement treatments: Perils and pitfalls for patients and providers

J Am Assoc Nurse Pract. 2025 Jan 1;37(1):4-7. doi: 10.1097/JXX.0000000000001037.

Abstract

As the demand for "quick-fixes" and instant gratification intensifies among consumers of the US health care delivery system, health care providers remain essential to ensuring patients receive safe, evidenced-based care. Erectile dysfunction is a common health condition affecting as many as 42% of US men. As such, it is unsurprising that American health care consumers affected by erectile dysfunction (ED) may be tempted by "quick fixes" to ameliorate their symptoms-particularly if such fixes are perceived to be less embarrassing, more accessible, and/or more affordable. Although multiple therapies for the treatment of ED are approved by the US Food and Drug Administration, unregulated and/or counterfeit treatments are abundantly available to health care consumers on the Internet and US retail settings. These unregulated treatments may take the form of over-the-counter supplements or tainted prescription medications from illegal Internet pharmacies. This clinical brief is a call to action for health care professionals to advocate for patient safety, educate patients, and champion evidence-based therapies approved for the treatment of erectile dysfunction.

MeSH terms

  • Counterfeit Drugs
  • Erectile Dysfunction* / drug therapy
  • Erectile Dysfunction* / therapy
  • Humans
  • Male
  • Nonprescription Drugs
  • United States

Substances

  • Counterfeit Drugs
  • Nonprescription Drugs