Drug Interaction Report
2 potential interactions and/or warnings found for the following 2 drugs:
- Fulvicin U/F (griseofulvin)
- telithromycin
Interactions between your drugs
griseofulvin telithromycin
Applies to: Fulvicin U/F (griseofulvin), telithromycin
MONITOR: Coadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of telithromycin, which is primarily metabolized by the isoenzyme. When telithromycin was given with the potent CYP450 3A4 inducer rifampin in repeated doses, telithromycin peak plasma concentration (Cmax) and systemic exposure (AUC) decreased on average by 79% and 86%, respectively. No data are available for use with other, less potent inducers. Subtherapeutic levels of telithromycin and loss of effect may occur. Enzyme activities usually return to normal 14 days after discontinuation of the inducing agent.
MANAGEMENT: The potential for diminished therapeutic effects of telithromycin should be considered when prescribed with CYP450 3A4 inducers. Pharmacologic response to telithromycin should be monitored closely during coadministration, and alternative treatment given if an interaction is suspected. Whenever possible, telithromycin should preferably not be used during or within 2 weeks after discontinuation of treatment with a CYP450 3A4 inducer.
References (2)
- (2004) "Product Information. Ketek (telithromycin)." Aventis Pharmaceuticals
- European Agency for the Evaluation of Medicinal Products. Committee for Proprietary Medicinal Products (2004) European Public Assessment Report Ketek (telithromycin) (Rev. 2) http:www.emea.eu.int/humandocs/Humans/EPAR/Ketek/Ketek.htm
Drug and food interactions
griseofulvin food
Applies to: Fulvicin U/F (griseofulvin)
MONITOR: Isolated case reports have suggested that the ingestion of alcohol during griseofulvin therapy may rarely cause disulfiram-like reactions, flushing, tachycardia, or increased effects of alcohol. The mechanism is unknown.
MANAGEMENT: Patients should be advised of the possibility of increased adverse effects or a disulfiram-like reaction.
References (3)
- "Product Information. Grifulvin V (griseofulvin)." Ortho McNeil Pharmaceutical
- (2002) "Product Information. Fulvicin P/G (griseofulvin)." Schering Corporation
- Cerner Multum, Inc. "Australian Product Information."
Therapeutic duplication warnings
No duplication warnings were found for your selected drugs.
Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
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Further information
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