WHO Pharmaceuticals Newsletter 2004, No. 06
(2004; 13 pages) Ver el documento en el formato PDF
Índice de contenido
Abrir esta carpeta y ver su contenidoREGULATORY MATTERS
Cerrar esta carpetaSAFETY OF MEDICINES
Ver el documentoCHOLINESTERASE INHIBITORS - Reports of cardiac arrhythmias
Ver el documentoCYCLOOXYGENASE-2 INHIBITORS - Plans to review all medicines in this class
Ver el documentoETHINYLESTRADIOL/CYPROTERONE - Increased risk of thrombosis
Ver el documentoHERBAL MEDICINES - Cardiovascular ADRs reported to Health Canada
Ver el documentoINFLUENZA VIRUS VACCINE - Interactions with drugs
Ver el documentoMEDROXY PROGESTERONE - Effect on bone mineral density
Ver el documentoPAMIDRONATE DISODIUM, ZOLEDRONIC ACID - Spontaneous reports of osteonecrosis of the jaw
Ver el documentoSELECTIVE SEROTONIN REUPTAKE INHIBITORS (SSRIs) - ADRAC reviews use in children and adolescents
Ver el documentoTERBINAFINE - Reports of blood dyscrasias
Ver el documentoTRICYCLIC ANTIDEPRESSANTS - Overdose risk
Ver el documentoFEATURE
 

TERBINAFINE - Reports of blood dyscrasias

Australia. ADRAC has received a total of 14 reports of blood dyscrasias associated with terbinafine, indicated for onychomycosis, in patients aged 35-84 years (median 65). Of these reports, seven were of agranulocytosis, five of neutropenia and two of pancytopenia, with a time to onset of between 4 and 10 weeks. Recovery was documented in 9 of the 14 reports and, in four cases, occurred within one week of terbinafine discontinuation. The Committee recommends that patients taking terbinafine for longer than one month should be advised to report any symptoms of possible infection, and that if symptoms develop, blood counts should be checked.

Reference:

Australian Adverse Drug Reactions Bulletin, Vol. 23, No.5, October 2004. Available on the Internet at www.tga.gov.au

Reports in WHO-file: Blood dyscrasias 1

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Última actualización: le 3 mayo 2013