WHO Drug Information Vol. 14, No. 4, 2000
(2000; 78 pages) Voir le document au format PDF
Table des matières
Ouvrir ce répertoire et afficher son contenuGeneral Policy Issues
Ouvrir ce répertoire et afficher son contenuVaccines and Biomedicines
Ouvrir ce répertoire et afficher son contenuGeneral Information
Fermer ce répertoireRegulatory and Safety Matters
Afficher le documentEtanercept: serious haematological reactions
Afficher le documentInfliximab: safety restrictions
Afficher le documentPhenylpropanolamine withdrawn from drug products
Afficher le documentLabelling revision for phenylpropanolamine
Afficher le documentPhenylpropanolamine advisory to consumers
Afficher le documentPhenylpropanolamine: strengthening of patient information
Afficher le documentLevacetylmethadol and cardiac disorders
Afficher le documentBovine-derived materials and vaccines: US recommendations
Afficher le documentProducts containing human albumin
Afficher le documentStavudine and didanosine: pregnancy advisory
Afficher le documentMethysergide and cardiac valvulopathy
Afficher le documentGreater control for cisapride
Afficher le documentNew combination drug for HIV
Afficher le documentTacrolimus for atopic dermatitis
Afficher le documentLetrozole approved for advanced breast cancer
Afficher le documentAlosetron withdrawn
Afficher le documentBasiliximab: hypersensitivity reactions
Afficher le documentBudipine: cardiac reactions
Afficher le documentCapecitabine: revised data sheet
Afficher le documentBenzathine penicillin: fatal mega-unit injections
Afficher le documentDisulfiram: hepatic reactions
Afficher le documentIsoniazid and rifampicin: severe skin reactions
Afficher le documentOmeprazole-induced interstitial nephritis
Afficher le documentOzagrel sodium: kidney function disorder
Afficher le documentDrug information to the public
Afficher le documentNorthern hemisphere influenza vaccine composition
Afficher le documentATC/DDD Classification (final)
Afficher le documentATC/DDD Classification (temporary)
Ouvrir ce répertoire et afficher son contenuHerbal Medicines
Ouvrir ce répertoire et afficher son contenuPublications and Sources of Information
 

Bovine-derived materials and vaccines: US recommendations

United States of America - The Center for Biologics Evaluation and Research (CBER) convened a meeting in July 2000 of the Transmissible Spongiform Encephalopathy Advisory Committee and the Vaccines and Related Biological Products Advisory Committee to discuss the status of vaccines which have been manufactured with bovinederived materials. No evidence exists that cases of variant Creutzfeldt-Jakob disease (vCJD) are related to the use of vaccines, and no cases of vCJD have been reported in the United States.

The Committees concluded that the risk of vCJD posed by vaccines in the United States was theoretical and remote. This conclusion was based on the inherent low risk of the bovine materials involved and/or the dilutions of materials during manufacture. The Committees concluded that the benefits of vaccination outweigh any remote risk of vCJD.

The Food and Drug Administration has requested manufacturers to replace bovine-derived materials obtained from countries where bovine spongiform encephalopathy (BSE) has been reported with materials from BSE-free countries. The Public Health Service recommends that all persons continue to be vaccinated according to current schedules.

Reference: Morbidity and Mortality Weekly Report, 49(50): 1137–1138 (2000). http://www.cdc.gov/mmwr

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Dernière mise à jour: le 3 mai 2013