WHO Drug Information Vol. 14, No. 3, 2000
(2000; 71 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 contenuCurrent Topics
Fermer ce répertoireRegulatory and Safety Matters
Afficher le documentMisoprostol and pregnancy: reminder of dangers
Afficher le documentSouthern hemisphere influenza vaccine composition
Afficher le documentZafirlukast: labelling changes
Afficher le documentThioridazine: major labelling modifications
Afficher le documentMesoridazine besylate: new warning
Afficher le documentLopinavir and ritonavir for HIV infection
Afficher le documentArsenic trioxide for leukaemia
Afficher le documentInternational plasma trafficking
Afficher le documentCardiac failure and pioglitazone hydrochloride
Afficher le documentNew dosing for didanosine
Afficher le documentAlosetron: guide and labelling improve risk detection
Afficher le documentMeningitis C vaccines
Afficher le documentMifepristone approval linked to stringent conditions
Afficher le documentProposed withdrawal of enrofloxacin in poultry
Ouvrir ce répertoire et afficher son contenuConsultative Document
Ouvrir ce répertoire et afficher son contenuRecent Publications and Sources of Information
Afficher le documentRecommended International Nonproprietary Names: List 44
Afficher le documentSelected WHO publications of related interest
 

New dosing for didanosine

The manufacturer of the nucleoside analogue reverse transcriptase inhibitor, didanosine (Videx®), has advised health care providers of a change in prescribing information. The results of a recent clinical trial have demonstrated that the treatment response rate of once-daily didanosine was significantly lower than in the comparator arm. Although once daily dosing is available, it should only be considered for adult patients whose management requires this administration.

It is therefore recommended that the more effective dosing frequency of didanosine is twice-daily.

Reference: Letter from Bristol-Myers Squibb Company, USA, dated 1 August 2000.

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Dernière mise à jour: le 3 mai 2013