Примери за използване на Metabolising на Английски и техните преводи на Български
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This is due to induction of metabolising enzymes by St John' s Wort.
Esomeprazole inhibits CYP2C19,the major esomeprazole metabolising enzyme.
No effect on hepatic metabolising enzymes was observed in humans receiving clopidogrel at the therapeutic dose.
This is due to the induction of drug metabolising enzymes by St John' s wort.
No effect on hepatic metabolising enzymes was observed in humans receiving clopidogrel at the therapeutic dose.
This decrease is probably due to auto-induction of metabolising liver enzymes.
The metabolising enzymes have not been fully investigated and slower metabolism(up to four-fold increased exposure) has been noted in some individuals.
This is due to the induction of metabolising enzymes by St John's wort.
Drug metabolising enzymes(and drug transporters) other than CYP3A4 involved in rolapitant hepatobiliary elimination remain to be elucidated.
This is due to the induction of drug metabolising enzymes by St John' s wort.
Dabrafenib is an inducer of metabolising enzymes which may lead to loss of efficacy of many commonly used medicinal products(see examples in section 4.5).
In vitro data indicate that eribulin is a mild inhibitor of the important drug metabolising enzyme CYP3A4.
John's wort due to induction of drug metabolising enzymes and/ or transport proteins by St.
The effect of high-dose AVONEX administration on P450-dependent metabolism in monkeys was evaluated andno changes in liver metabolising capabilities were observed.
Dabrafenib is a substrate for the metabolising enzymes CYP2C8 and CYP3A4, while the active metabolites hydroxy-dabrafenib and desmethyl-dabrafenib are CYP3A4 substrates.
In vitro data indicate that ledipasvir may be a weak inducer of metabolising enzymes such as CYP3A4, CYP2C and UGT1A1.
Based on in vitro data on metabolising enzymes and transporters delafloxacin possesses a low potential to alter the disposition of other medicinal products(see section 5.2).
Like the other B vitamins,it supports energy production by aiding in the metabolising of fats, carbohydrates, and proteins.
GS-563117 is not an inhibitor of the metabolising enzymes CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6 or UGT1A1, or of the transporters P-gp, BCRP, OATP1B1, OATP1B3, OAT1, OAT3, or OCT2.
Bimatoprost is biotransformed by anyof multiple enzymes and pathways, and no effects on hepatic drug metabolising enzymes were observed in preclinical studies.
Concomitant use of enzalutamide with medicinal products that are sensitive substrates of many metabolising enzymes or transporters(see section 4.5) should generally be avoided if their therapeutic effect is of large importance to the patient, and if dose adjustments cannot easily be performed based on monitoring of efficacy or plasma concentrations.
These occurred at doses representing at least 25 times the exposure seen in humans receiving the clinical dose of 75 mg/day andwere a consequence of an effect on hepatic metabolising enzymes.
In vitro data indicated that idelalisib is not an inhibitor of the metabolising enzymes CYP1A2, CYP2B6, CYP2C9, CYP2C19, CYP2D6, CYP3A, or UGT1A1, or of the transporters OAT1, OAT3, or OCT2.
These occurred at doses representing at least 25 times the exposure seen in humans receiving the clinical dose of 75 mg/day andwere a consequence of an effect on hepatic metabolising enzymes.
Concomitant use of dabrafenib with medicinal products that are sensitive substrates of certain metabolising enzymes or transporters(see section 4.5) should generally be avoided if monitoring for efficacy and dose adjustment is not possible.
These occurred at doses representing at least 25 times the exposure seen in humans receiving the clinical dose of 75 mg/day andwere a consequence of an effect on hepatic metabolising enzymes.
Plasma levels of efavirenz can be reduced by concomitant use of St. John's wort due to induction of drug metabolising enzymes and/or transport proteins by St. John's wort.
These occurred at doses representing at least 25 times the exposure seen in humans receiving the clinical dose of 75 mg/day andwere a consequence of an effect on hepatic metabolising enzymes.
In repeated-dose toxicity studies, dose-related liver changes(weight, centrilobular hypertrophy, occasionally necrosis),induction of hepatic drug metabolising enzymes and slightly decreased erythron parameters were seen in mice, rats and dogs.
Interaction with other medicinal products and other forms of interaction No formal drug interaction studies have been performed, as no drug interactions are expected via cytochrome P450 enzymes,other metabolising enzymes or transporters.