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Reporting undesirable side-effects

Pharmacovigilance

"Please find here forms to report adverse drug reactions. The second form is for reporting adverse reactions to antidotes and antivenoms only."

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MU101_20_001d_FO Meldung einer vermuteten unerwünschten Arzneimittelwirkung (UAW) (23.10.2009 | 278 kb | doc)

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MU101_20_004d_FO UAW Antidota Antivenine (08.01.2010 | 375 kb | doc)

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MU101_21_012e_FO Form to be submitted with every individual case safety report (spontaneous or orginating from clinical trials) (14.05.2009 | 159 kb | doc)

TAM-Vigilance

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MU101_40_001d_FO_web_UAW_Tamvigilance (30.11.2009 | 317 kb | doc)

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Meldung unerwünschter Tierarzneimittelwirkungen (30.11.2009 | 54 kb | pdf)

Haemovigilance

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MU101_10_021d_FO Haemovigilance Meldung Transfusionsreaktion (02.03.2009 | 369 kb | doc)

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MU101_10_023d_FO Haemovigilance Meldung Transfusionsfehler / Near Miss (02.03.2009 | 309 kb | doc)

Materiovigilance

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MU101_30_005e_FO Field Safety Corrective Action (14.07.2010 | 286 kb | doc)

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Human medicines

Complementary and herbal medicines

Veterinary medicines

Blood and blood components

Medical devices

Transplant products

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Materiovigilance

Swissmedic • Swiss Agency for Therapeutic Products • Hallerstrasse 7 • P.O. Box • CH-3000 Bern 9
P: +41 31 322 02 11 • F: +41 31 322 02 12 • Disclaimer

http://www.swissmedic.ch/00397/index.html?lang=en