I had a very good idea for drugs are withdrawn from the market more quickly, since the side effects are more important than the service: should every doctor has his computer with a direct portal pharmacovigilance works with the health professional card and the card life the patient. In fact, it seems that everything is being done to ensure that the statements were not made. For example when I wanted to report an adverse reaction due to champix (depression followed by a stay in a psychiatric clinic with intense desires for suicide) it was the intention:
- I first put a little time to find The pharmacovigilance center nearest;
_ it took I print the paper reporting;
- I then sent by mail because they did not accept online;
- two weeks later they asked me more information.
I proposed to the lady of the social security (the social security web doctor put me on to my work stoppage online) and she said it was not within its purview.
So who is it spring? Will we still have much trouble to report any side effects? How many adverse effects did not I reported (as big anemia ibuprofen while suffering from a gastrointestinal type, sending it to hospital, for example)?
If someone can do something about my bed, let him please.
- I first put a little time to find The pharmacovigilance center nearest;
_ it took I print the paper reporting;
- I then sent by mail because they did not accept online;
- two weeks later they asked me more information.
I proposed to the lady of the social security (the social security web doctor put me on to my work stoppage online) and she said it was not within its purview.
So who is it spring? Will we still have much trouble to report any side effects? How many adverse effects did not I reported (as big anemia ibuprofen while suffering from a gastrointestinal type, sending it to hospital, for example)?
If someone can do something about my bed, let him please.
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