Examples of using To induction in English and their translations into Finnish
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Medicine
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Colloquial
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Official
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Financial
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Ecclesiastic
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Official/political
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Computer
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Programming
This effect may be due to induction of bupropion metabolism.
Dolutegravir Not studied, a similar reduction in exposure as observed with efavirenz is expected, due to induction.
This effect may be due to induction of bupropion metabolism.
However, increased methadone dose may be necessary when concomitantly administered for a longer period of time due to induction of metabolism by ritonavir.
This is most likely due to induction of CYP3A4 by bosentan.
The premedication dose of dexmedetomidine is 125- 375 micrograms/square metre body surface area,administered 20 minutes prior to induction for procedures requiring anaesthesia.
This is due to induction of drug metabolising enzymes by St John' s wort.
Plasma levels of cinacalcet may be lower in smokers due to induction of CYP1A2-mediated metabolism.
This is due to induction of drug metabolising enzymes and/or transport proteins by St. John's wort.
Interaction with indinavir/ ritonavir not studied Morphine levels may be decreased due to induction of glucuronidation by coadministered ritonavir.
Dolutegravir Not studied, decrease expected due to induction of UGT1A1 and CYP3A enzymes, a similar reduction in exposure as observed with carbamazepine is expected.
Smoking: Clearance of cinacalcet is higher in smokers than in non-smokers, likely due to induction of CYP1A2- mediated metabolism.
Morphine Morphine levels may be decreased due to induction of glucuronidation by co-administered ritonavir dosed as an antiretroviral agent or as a pharmacokinetic enhancer.
Repeated-dose toxicity testing andembryo-fetal toxicity studies are impractical due to induction of, and interference with antibodies.
Methadone1 5, single dose 500 q12h,↓ 36%↓ 38% Increased methadone dose may be necessary when concomitantly administered with ritonavir dosed as an antiretroviral agent or as a pharmacokinetic enhancer due to induction of glucuronidation.
Repeated dose toxicity testing andembryo-foetal toxicity studies are impracticable due to induction of, and interference with antibodies.
Combined hormonal contraceptives have been shown to significantly decrease plasma concentrations of lamotrigine when co-administered due to induction of lamotrigine glucuronidation.
In a study in 10 male volunteers, rifampicin increased lamotrigine clearance and decreased lamotrigine half-life due to induction of the hepatic enzymes responsible for glucuronidation.
It can also be used as maintenance treatment in patients whose follicular lymphoma has come back after previous treatment,provided that the lymphoma has responded to induction treatment an earlier round of treatment.
Studies of repeated dose toxicity, genotoxicity, and toxicity to reproduction in animals are impracticable due to induction of and interference by developing antibodies to heterologous proteins.
The concomitant systemic administration of phenytoin to patients receiving high-dose busulfan has been reported to increase busulfan clearance, due to induction of glutathion-S-transferase.
Experimental evidence shows that the mechanism(s)of action by which celecoxib leads to tumour death may be related to induction of apoptosis and inhibition of angiogenesis.
Lamotrigine: Combined hormonal contraceptives have been shown to significantly decrease plasma concentrations of lamotrigine when coadministered likely due to induction of lamotrigine glucuronidation.