Voorbeelden van het gebruik van Fluvastatin in het Engels en hun vertalingen in het Nederlands
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The interactions between pitavastatin and fluvastatin and Viekirax have not been investigated.
Other statins that are not CYP3A4 substrates(pravastatin and fluvastatin) can be co-administered with Ketoconazole HRA.
Theoretically, Viekirax with and without dasabuvir is expected to increase the exposure to pitavastatin and fluvastatin.
HMG Co-A Reductase Inhibitors Atorvastatin, Fluvastatin, Lovastatin, Pravstatin, Rosuvastatin, Simvastatin.
pravastatin or fluvastatin is recommended.
The results suggested that cerivastatin was associated with the lowest risk of myopathy whilst fluvastatin had the highest.
This indicates that co-administration of regorafenib may increase the plasma concentrations of other concomitant BCRP substrates e.g. methotrexate, fluvastatin, atorvastatin.
reductase inhibitor is indicated, pravastatin or fluvastatin is recommended with careful monitoring see section 4.5.
will affect the pharmacokinetics of other statins e.g., atorvastatin, fluvastatin, pravastatin, rosuvastatin.
Although not studied, there is a potential for an increase in pravastatin or fluvastatin exposure when co- administered with protease inhibitors.
The use of another HMG- CoA reductase inhibitor which does not undergo metabolism by CYP3A such as pravastatin or fluvastatin is recommended.
rosuvastatin and fluvastatin.
Based on known metabolic profiles, clinically significant interactions are not expected between Kaletra and fluvastatin, dapsone, trimethoprim/ sulfamethoxazole,
Fluvastatin, and rosuvastatin are metabolised by CYP2C9
The OATP1B1 inhibition could result in increased exposure of medicinal products such as statins(atorvastatin, fluvastatin, pitavastatin, and lovastatin),
drugs transported by these transporters such as fluvastatin, pravastatin, rosuvastatin,
pravastatin or fluvastatin is recommended because their metabolism is not dependent on CYP3A4
reductase inhibitor is indicated, pravastatin or fluvastatin is recommended because their metabolism is not dependent on CYP 3A4 and interactions are not expected with protease inhibitors.
Fluvastatin used to treat high cholesterol.
Fluvastatin is partially metabolised by CYP2C9.