European Medicines Agency asks for us!

[anacleta]

The European Medicines Agency (EMA) recently discussed, and is currently discussing, for the first time, persistent sexual dysfunction from SSRI / SNRI and the possibility of adding indications on drug labels.

The EMA seems to have been driven in particular by the Citizen Petition written by David Healy and undersigned by all researchers who have so far been interested in investigating the problem in the medical literature.

The EMA has asked us with PSSD to fill out a short questionnaire with name and surname, through David Healy.

These are the essential steps:

1- compile report on Rxisk: https://rxisk.org/experiencing-a-drug-side-effect/

2- send an email to Healy giving the availability to authenticate with name and surname (and be contacted by the EMA if necessary): david.healy@rxisk.org

3- Healy will answer attaching another short questionnaire to fill in with name and surname, requested by the EMA.
The EMA must receive them BY THE END OF DECEMBER.

ps. David Healy updates by email those with PSSD who have completed the Rxisk report.

[Snake]

Thank God. I assume that everyone will compile that report and contact dr Healy. Come on!

[lw77]

Guys, this is our chance, we have nothing to loose, please fill the report on RxISK, if we miss this chance and we fail to demonstrate our problem, the agencies can say (with reason) that they had evaluated the problem and that there were not sufficient evidences. At that time we will not be allowed to complaint anymore, because they gave us the chance and we did nothing.
Don't worry to give names and surnames because they will remain confidential.
Let's make our voices be heard.

[Snake]

Ok, I have done everything that anacleta has written.
Waiting for others!

[chemistry]

Thanks for reminding me - done!

Everyone on this forum needs to get this done this is a huge opportunity for us.

[Dead]

Submitted.

[zadig777]

when will they publish this?

[dann888]

Thanks. Submitted!!!

[omar90]

I think a lot of us are underestimating how big an opportunity this is for us. This could help get recognition from the EMA and FDA, two of the biggest and most influential drug regulatory bodies in the World. Please submit !!

[Zolofthater420]

I did. Maybe many people do but don't write it here.