Each european country provides a regulatory authority which is responsible for human medicines. All these agencies can report to EMA (European Medicines Agency). In most of the countries, side effects reporting can be done on the national web site of the agency even when you are a patient.
Parce que l'utilisation du cytotec (misoprostol) pour déclencher les accouchements ne s'arrête pas à nos frontières, nous avons référencé ci-dessous l'ensemble des agences nationales du médicament avec les adresses web des pages de déclaration :
Because cytotec (misoprostol) for labour induction is used worldwide, we listed here most of the national medicines agencies declaration forms:
Europe :
Autriche / Austria : AGES (Austrian Agency for Health and Food Safety)

Belgique / Belgium : FAMHP (Federal Agency for Medicines and Health Products)

Bulgarie / Bulgaria : BDA (Bulgarian Drug Agency)

Chypre / Cyprus : Ministry of Health - Pharmaceutical Services

République Tchèque / Czech Republic : SÚKL (State Institute for Drug Control)

Danemark / Denmark : Sundheds styrelsen (Danish Health and Medicines Authority)

Estonie / Estonia : SAM (State Agency of Medicines)

Finlande / Finland : FINEA (Finnish Medicines Agency)

France : ANSM (National Agency for the Safety of Medicine and Health Products)

Allemagne / Germany : BfArM (Federal Institute for Drugs and Medical Devices)

Grèce / Greece : EOΦ (National Organization for Medicines)

Hongrie / Hungary : OGYI (National Institute of Pharmacy)

Iceland / Iceland : IMA (Icelandic Medicines Agency)

Irlande / Ireland : IMB (Irish Medicines Board)

Italie / Italy : AIFA (Italian Medicines Agency)

Létonie / Latvia : ZVA (State Agency of Medicines)

Liechtenstein : LLV (Office of Health / Department of Pharmaceuticals)

Lituanie / Lithuania : VVKT (State Medicines Control Agency)

Luxembourg : Ministry of Health

Malte / Malta : AWTORITA DWAR IL-MEDICINI (Medicines Authority)

Pays-bas / Netherlands : CBG MEB (Medicines Evaluation Board)

Norvège / Norway : Statens legemiddelverk (Norwegian Medicines Agency)

Pologne / Poland : Główny Inspektorat Farmaceutyczny (Main Pharmaceutical Inspectorate)

Portugal : Infarmed (National Authority of Medicines and Health Products)

Roumanie / Romania : ANM (National Medicines Agency)

Slovaquie / Slovakia : ŠÚKL (State Institute for Drug Control)

Slovénie / Slovenia : jazmp (Agency for Medicinal Products and Medical Devices of the Republic of Slovenia)

Espagne / Spain : AEMPS (Spanish Agency for Medicines and Health Products)

Suède / Sweden : Läkemedelsverket (Medical Products Agency)

Royaume-Uni / United Kingdom : MHRA (Medicines and Healthcare Products Regulatory Agency)

Reste du monde / worldwide :
Etats-Unis d'Amérique / USA : FDA (Food & Drug Administration)

Suisse / Switzerland : SwissMedic

A suivre...
To be continued...