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Is Online ED Treatment Legitimate and Safe?

Updated over a week ago

Online ED Treatment Safety


Online erectile dysfunction (ED) treatment has become increasingly accessible through telemedicine and direct-to-consumer (DTC) platforms, offering convenience and privacy for men who may be reluctant to seek in-person care. The legitimacy and safety of these services depend on several factors, including adherence to evidence-based clinical guidelines, regulatory oversight, and the quality of patient evaluation and counseling.

Legitimacy of Online ED Treatment

Telemedicine for men's sexual health, including ED, is recognized as a legitimate care modality by major professional societies such as the American Urological Association (AUA) and the Sexual Medicine Society of North America, provided that care is delivered in accordance with established clinical standards and ethical guidelines.[1][2] The COVID-19 pandemic accelerated the adoption of telehealth, and studies have shown that, when properly regulated, telemedicine can improve access to care, patient satisfaction, and health outcomes for select conditions, including ED.[1][3][4] The Society of General Internal Medicine and the American Medical Association have also issued guidance supporting telemedicine as a complement to traditional care, provided that patient safety, privacy, and quality are maintained.[5][3][4]

Safety and Quality Considerations

The safety of online ED treatment is closely linked to the thoroughness of the clinical evaluation. The AUA recommends that all men presenting with ED undergo a comprehensive medical, sexual, and psychosocial history, physical examination, and selective laboratory testing to identify underlying causes and comorbidities.[2][6] While some telemedicine platforms employ structured questionnaires and virtual visits to assess ED, recent analyses indicate that the quality of information and counseling varies widely between platforms, with larger, more established services generally providing higher-quality content.[7] However, DTC platforms that rely solely on questionnaires may overlook important comorbidities, such as hypogonadism, diabetes, dyslipidemia, or even subfertility, which would typically be identified during an in-person evaluation.[8][6] This is particularly relevant for younger men, in whom ED may be a marker of significant underlying pathology.[8][6]

A retrospective study comparing state-regulated internet prescribing systems to traditional care found that, for phosphodiesterase type 5 (PDE5) inhibitors, safety outcomes were non-inferior between the two models, provided that appropriate screening protocols were followed.[9] However, the study also highlighted the importance of standardized diagnostic questions and medication counseling, which were more consistently applied in the e-medicine system than in traditional care.[9] Other research has shown that DTC telemedicine visits for ED are most commonly used by younger, urban, and technologically savvy patients, often outside of normal business hours, and may address barriers to care such as stigma or inconvenience.[10]

Regulatory and Ethical Oversight

The regulatory landscape for online ED treatment is evolving. The Drug Enforcement Administration (DEA) and the Food and Drug Administration (FDA) have established special telemedicine prescribing registrations and oversight mechanisms to ensure that controlled substances, including certain ED medications, are prescribed safely and appropriately.[11] The Drug Quality and Security Act (DQSA) and state pharmacy boards provide additional oversight for compounded medications, which may be offered by some online platforms.[12][13][14][15][16][17][18][19][20][21][22][23] The American Diabetes Association and other professional societies caution against the use of non-FDA-approved compounded medications except in the context of documented shortages, due to concerns about safety, quality, and effectiveness.[16]

Ethical practice in telemedicine requires that clinicians ensure patient privacy, informed consent, and continuity of care, and that they recognize the limitations of remote evaluation.[5][4] The American Medical Association's Code of Medical Ethics and the Society of General Internal Medicine both emphasize the need for appropriate use of telemedicine, integration with in-person care when necessary, and ongoing monitoring for adverse outcomes.[5][3][4]

Summary and Clinical Recommendations

- Online ED treatment can be legitimate and safe when delivered by licensed clinicians following evidence-based guidelines, with appropriate regulatory oversight and patient safeguards.[1][2][5][3][9][4]

- Comprehensive evaluation—including history, risk assessment, and selective laboratory testing—remains essential to identify underlying causes and comorbidities.[2][8][6]

- The quality of care and information varies between platforms; larger, established services tend to provide more reliable counseling, but all platforms may miss important diagnoses without in-person assessment.[7][8]

- Regulatory oversight, including DEA and FDA requirements, is critical for the safe prescribing of ED medications and compounded products.[12][13][14][15][16][17][18][19][20][21][22][23][11]

- Telemedicine should be integrated with traditional care, and patients with complex or refractory ED should be referred for in-person evaluation.[2][8][6]

In summary, online ED treatment is a legitimate and increasingly utilized care option, but its safety and effectiveness depend on adherence to clinical standards, regulatory compliance, and the ability to recognize when in-person evaluation is warranted.

References

  1. Sexual Medicine Society of North America (SMSNA)/American Urological Association (AUA) Telemedicine and Men's Health White Paper. Khera M, Bernie HL, Broderick G, et al. The Journal of Sexual Medicine. 2024;:qdad151. doi:10.1093/jsxmed/qdad151.

  2. Erectile Dysfunction: AUA Guideline. Burnett AL, Nehra A, Breau RH, et al. The Journal of Urology. 2018;200(3):633-641. doi:10.1016/j.juro.2018.05.004.

  3. Telehealth Policy, Practice, and Education: A Position Statement of the Society of General Internal Medicine. Chen A, Ayub MH, Mishuris RG, et al. Journal of General Internal Medicine. 2023;38(11):2613-2620. doi:10.1007/s11606-023-08190-8.

  4. Telehealth. Tuckson RV, Edmunds M, Hodgkins ML. The New England Journal of Medicine. 2017;377(16):1585-1592. doi:10.1056/NEJMsr1503323.

  5. Ethical Practice in Telehealth and Telemedicine. Chaet D, Clearfield R, Sabin JE, Skimming K. Journal of General Internal Medicine. 2017;32(10):1136-1140. doi:10.1007/s11606-017-4082-2.

  6. Current Diagnosis and Management of Erectile Dysfunction. McMahon CG. The Medical Journal of Australia. 2019;210(10):469-476. doi:10.5694/mja2.50167.

  7. Quality of Health Information Presented in Direct-to-Consumer Telepharmacies for the Treatment of Patients With Erectile Dysfunction. Mittauer DJ, Jhaveri HF, Schroeder TE, Peterson AC. Urology. 2025;201:46-51. doi:10.1016/j.urology.2025.04.018.

  8. Safety of Prescribing PDE-5 Inhibitors via E-Medicine vs Traditional Medicine. Munger MA, Stoddard GJ, Wenner AR, et al. Mayo Clinic Proceedings. 2008;83(8):890-6. doi:10.4065/83.8.890.

  9. Comparison of Direct-to-Consumer Telemedicine Visits With Primary Care Visits. Jain T, Mehrotra A. JAMA Network Open. 2020;3(12):e2028392. doi:10.1001/jamanetworkopen.2020.28392.

  10. Telemedicine Special Registrations for Controlled Substances. Kannarkat JT, Torous J, Kannarkat JT. JAMA Health Forum. 2025;6(7):e252795. doi:10.1001/jamahealthforum.2025.2795.

  11. The Practice of Compounding, Associated Compounding Regulations, and the Impact on Dermatologists. Quertermous J, Desai S, Harper J, et al. Journal of Drugs in Dermatology : JDD. 2018;17(7):s17-s22.

  12. Compounding Pharmacy Conundrum: "We Cannot Live Without Them but We Cannot Live With Them" According to the Present Paradigm. Guharoy R, Noviasky J, Haydar Z, Fakih MG, Hartman C. Chest. 2013;143(4):896-900. doi:10.1378/chest.13-0212.

  13. Update on Medical and Regulatory Issues Pertaining to Compounded and FDA-approved Drugs, Including Hormone Therapy. Pinkerton JV, Pickar JH. Menopause (New York, N.Y.). 2016;23(2):215-23. doi:10.1097/GME.0000000000000523.

  14. Sterile Compounding: Clinical, Legal, and Regulatory Implications for Patient Safety. Qureshi N, Wesolowicz L, Stievater T, Lin AT. Journal of Managed Care & Specialty Pharmacy. 2014;20(12):1183-91. doi:10.18553/jmcp.2014.20.12.1183.

  15. Compounded GLP-1 and Dual GIP/GLP-1 Receptor Agonists: A Statement From the American Diabetes Association. Neumiller JJ, Bajaj M, Bannuru RR, et al. Diabetes Care. 2025;48(2):177-181. doi:10.2337/dci24-0091.

  16. How Gaps in Regulation of Compounding Pharmacy Set the Stage for a Multistate Fungal Meningitis Outbreak. Teshome BF, Reveles KR, Lee GC, Ryan L, Frei CR. Journal of the American Pharmacists Association : JAPhA. 2014 Jul-Aug;54(4):441-5. doi:10.1331/JAPhA.2014.14011.

  17. Distinguishing Between Compounding Facilities and the Development of the 503B Bulk Drug Substance List. Gianturco SL, Mattingly AN. Journal of the American Pharmacists Association : JAPhA. 2021 Jan-Feb;61(1):e8-e11. doi:10.1016/j.japh.2020.06.024.

  18. Increased Regulation of Medication Compounding by State Boards of Pharmacy. Reynolds KA, Ibrahim SA, Hellquist KA, Poon E, Alam M. Archives of Dermatological Research. 2022;314(8):787-790. doi:10.1007/s00403-021-02290-3.

  19. Pharmacy Compounding of High-Risk Level Products and Patient Safety. Mullarkey T. American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists. 2009;66(17 Suppl 5):S4-13. doi:10.2146/ajhp0108b.

  20. Outsourcing Facilities and Their Place in the U.S. Drug Supply Chain. Gianturco SL, Yoon S, Yuen MV, Mattingly AN. Journal of the American Pharmacists Association : JAPhA. 2021 Jan-Feb;61(1):e99-e102. doi:10.1016/j.japh.2020.07.021.

  21. The Role of Outsourcing Facilities in Overcoming Drug Shortages. Mattingly AN. Journal of the American Pharmacists Association : JAPhA. 2021 Jan-Feb;61(1):e110-e114. doi:10.1016/j.japh.2020.08.027.

  22. A Pharmacist-Driven Food and Drug Administration Incident Surveillance and Response Program for Compounded Drugs. Janusziewicz AN, Glueck SN, Park SY, et al. American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists. 2021;78(15):1438-1443. doi:10.1093/ajhp/zxab176.

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