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Printed 23/05/2012
Url http://laegemiddelstyrelsen.dk/en/topics/side-effects-and-trials/side-effects/report-a-side-effect-or-incident
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Side effects and trials
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Side effects and trials
Side effects
Report a side effect or incident
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Side effects and trials
Side effects
Report a side effect or incident
Humans
Animals
Blood and blood products
Tissues and cells
Clinical trials
Registration and monitoring
Companies' reporting of side effects
Positive experience with ADR reporting
Drug Analysis Prints: reported adverse reactions
Medicines with stricter reporting requirements for doctors, dentists and veterinarians
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The Council for Adverse Drug Reactions
The EU Pharmacovigilance Working Party (PhVWP)
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Adverse incidents
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Report a side effect or incident
Here you can report:
side effects in humans
side effects in animals
side effects and adverse incidents involving blood and blood products
side effects and adverse incidents involving tissues and cells
adverse reactions in clinical trials
http://www.dkma.dk/visUKLSArtikel.asp?artikelID=1519
Documents and pages
15 September 2010
React to serious and unexpected side effects
The newsletter Danish Pharmacovigilance Update
Links
Authorised medicinal products (in Danish only)
Updated 21 May 2012