Re: Report PSSD to the FDA

[Guest guest]

>> http://www.fda.gov/cder/aers/default.htm>

EU citizens should report PSSD to the European Union Health Commission:

http://ec.europa.eu/dgs/health_consumer/index_en.htm

http://www.eurohealthnet.eu/index.php?option=com_content & task=blogsection & id=11 & Itemid=169

Also there is the European Agency for the Evaluation of Medicinal Products:

http://www.emea.europa.eu/

[Guest guest]

And every nation has its own governmental drug evaluation commission,

related tot the health department.

> EU citizens should report PSSD to the European Union Health Commission:

> http://ec.europa.eu/dgs/health_consumer/index_en.htm

[Guest guest]

OK. Let's make a list of them. I like to post this same thing from

time to time(FDA) for new members. Having a complete list would be

much better.

> > EU citizens should report PSSD to the European Union Health

Commission:

> > http://ec.europa.eu/dgs/health_consumer/index_en.htm

>

[Guest guest]

United Kingdom residents

Report your PSSD SSRI drug side-effects (also providing the PSSD wikipedia link: http://en.wikipedia.org/wiki/PSSD ) to the UK Medicines and Healthcare products Regulatory Agency:

Reporting suspected adverse drug reactions

A side effect from a medicine? Report it using Yellow Card.

If you wish to report a side effect of a medicine, please click on the Yellow Card button below to go to the online reporting site. Anybody from the United Kingdom can report this way.

Go to the online reporting site for the Yellow Card Scheme (opens in a new window)

The Yellow Card Scheme is run by the MHRA and the Commission on Human Medicines (CHM), and it is used to collect information from anybody, health professionals and the general public, on suspected side effects or adverse drug reactions (ADRs) from a medicine.The continued success of the Yellow Card Scheme depends on the willingness of people to report suspected adverse drug reactions.We collect Yellow Card reports from anyone from the UK on:

prescription medicines herbal remedies over-the-counter (OTC) medicines.

We also collect reports on ADRs suspected to be caused by unlicensed medicines in cosmetic treatments.

If you wish to report an adverse incident involving a medical device, to report an adverse blood reaction/event or report a counterfeit product, please use one of the methods described below:

Information for the Pharmaceutical IndustryInformation for pharmaceutical companies on the reporting of suspected adverse drug reaction (ADR) is available in the following section:

› Reporting suspected adverse drug reactions: Information for the Pharmaceutical Industry

http://www.mhra.gov.uk/Safetyinformation/Reportingsafetyproblems/Medicines/Reportingsuspectedadversedrugreactions/index.htm

> > > EU citizens should report PSSD to the European Union Health> Commission:> > > http://ec.europa.eu/dgs/health_consumer/index_en.htm> >>