WHO Pharmaceuticals Newsletter 2002, No. 04
(2002; 19 pages) Voir le document au format PDF
Table des matières
Fermer ce répertoireRegulatory matters
Afficher le documentACETYL-SALICYLIC ACID - New advice on aspirin use in children under 16
Afficher le documentACETYL-SALICYLIC ACID - Warning about incorrect information on new approved uses
Afficher le documentCABERGOLINE AND OTHERS - Revised package inserts
Afficher le documentEDARAVONE - Warnings about acute renal failure included in package insert
Afficher le documentERGOTAMINE TARTRATE AND CAFFEINE SUPPOSITORIES - Peripheral ischaemia with CYP 3A4 inhibitors
Afficher le documentGAMELONIC ACID - Withdrawal of marketing authorizations
Afficher le documentGEFITINIB - Reports of interstitial pneumonia may prompt review
Afficher le documentGEFITINIB - Revised product label to include interstitial pneumonia in the warning section
Afficher le documentIMATINIB - Additional adverse reactions reported
Afficher le documentISOTRETINOIN - Labelling changes
Afficher le documentLEPIRUDIN - Fatal anaphylactic reactions
Afficher le documentMEFLOQUINE - Contraindicated for prophylaxis in patients with major psychiatric disorders
Afficher le documentPARECOXIB - Risk of serious hypersensitivity and skin reactions
Afficher le documentPAROXETINE - Change in patient leaflet wording
Afficher le documentPHLEBOTONICS - Spain reassesses risk-benefit of oral vascular disorder therapies
Afficher le documentPIPER METHYSTICUM - Update on regulatory measures on kava products
Afficher le documentRABEPRAZOLE - Adverse reactions section updated
Afficher le documentSERTINDOLE - Move to reintroduce
Afficher le documentSLIM 10 - Withdrawal due to presence of undeclared substances
Afficher le documentTAMOXIFEN - Important safety information
Afficher le documentTICLOPIDINE - Physicians urged to conduct medical tests
Afficher le documentTRASTUZUMAB - Cardiotoxicity highlighted
Afficher le documentUROKINASE - Product reintroduced with important safety information update
Ouvrir ce répertoire et afficher son contenuSafety of medicines
Ouvrir ce répertoire et afficher son contenuDrugs of current interest
Ouvrir ce répertoire et afficher son contenuFeature
Afficher le documentEvents & announcements
 

RABEPRAZOLE - Adverse reactions section updated

Japan. One death suspected to be caused by interstitial pneumonia in a patient treated with sodium rabeprazole (Pariet) has been reported by the manufacturer in Japan. Based on this and other related reports the Japanese Ministry of Health and Labour Welfare has advised the company to add interstitial pneumonia to the Clinically Significant Adverse Reactions section in the product insert for rabeprazole (Pariet). Rabeprazole is a proton pump inhibitor that was launched in the Japanese market in 1997 and is used by as many as 500,000 patients a year.

Reference:
Pharma Japan 1802/8 July 2002.

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Dernière mise à jour: le 3 mai 2013