Osilodrostat and Alcohol/Food Interactions
There is 1 alcohol/food/lifestyle interaction with osilodrostat.
Caffeine Osilodrostat
Moderate Drug Interaction
MONITOR: Coadministration with osilodrostat may increase the plasma concentrations of drugs that are metabolized by CYP450 1A2, 2C19, 2D6, and/or 3A4. Osilodrostat has been shown to be a moderate inhibitor of CYP450 1A2, a mild to borderline moderate inhibitor of CYP450 2C19, and a weak inhibitor of CYP450 2D6 and 3A4. In a pharmacokinetic study with 20 healthy volunteers using a single 50 mg dose of osilodrostat and a probe drug cocktail, osilodrostat increased the exposures to caffeine (CYP450 1A2 substrate), omeprazole (CYP450 2C19 substrate), dextromethorphan (CYP450 2D6 substrate), and midazolam (CYP450 3A4/5 substrate) by 2.5-, 1.9-, 1.5- and 1.5-fold, respectively.
MANAGEMENT: Caution is advised when osilodrostat is used concurrently with drugs that are substrates of CYP450 1A2, 2C19, 2D6 and/or 3A4, particularly those with a narrow therapeutic range. Dosage adjustments as well as clinical and laboratory monitoring may be appropriate for some drugs whenever osilodrostat is added to or withdrawn from therapy.
References (3)
- (2020) "Product Information. Isturisa (osilodrostat)." Recordati Rare Diseases Inc
- (2022) "Product Information. Isturisa (osilodrostat)." (Obsolete) Recordati Rare Diseases Australia Pty Ltd, ISTURISA PI v1.1
- (2021) "Product Information. Isturisa (osilodrostat)." Recordati Rare Diseases UK Ltd
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Osilodrostat drug interactions
There are 589 drug interactions with osilodrostat.
Osilodrostat disease interactions
There are 4 disease interactions with osilodrostat which include:
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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. |
Further information
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