Report Your Symptoms

Reporting post-SSRI sexual dysfunction (PSSD) to health authorities creates an official record that contributes to global recognition of the condition. Follow the steps below. Each report that you file matters.

1
Use the Correct Term & Code

Most report forms only give you a free-text field for the reaction, so they won't prompt you for a code on their own. Always type the exact term below, not "low libido" or "sexual side effects," then add the MedDRA code yourself in the notes or comments field. This is what lets health authorities group your report together with every other PSSD case instead of losing it among generic complaints.

Term to use
post-SSRI sexual dysfunction
MedDRA code to add yourself
10086208

Use the term as the reaction, condition, or diagnosis name, and add the code in the notes or comments field. These are the officially recognized identifiers regulators search for.

2
Local Reporting
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3
Global: FDA
US FDA MedWatch
The FDA accepts reports from individuals worldwide. This is the most critical global database for drug safety monitoring.
Report to US FDA →
4
Global: RxISK
RxISK Database
A dedicated independent database for patients to report side effects and research drug safety data collectively.
Report to RxISK →
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Reporting to all relevant bodies ensures your experience contributes to the global safety profile of the medication. If you need assistance, contact our support team.