Exemple de utilizare a Known to induce în Engleză și traducerile lor în Română
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Medicinal products known to induce bradycardia.
In addition, caution should be exercised when administering Possia concomitantly with medicinal products known to induce bradycardia.
It is known To induce renal cell tumors.
Docetaxel is metabolised by CYP3A4 andprednisone is known to induce CYP3A4.
The formula is not known to induce any negative side effects or contraindications.
Caution should be used with medicinal products known to induce PR prolongations.
Administration of pomalidomide in smokers, with smoking tobacco known to induce the CYP1A2 isoform, had no clinically relevant effect on exposure to pomalidomide compared to that exposure to pomalidomide observed in non-smokers.
Lenalidomide is structurally related to thalidomide, which is known to induce severe peripheral neuropathy.
Administering paclitaxel concomitantly with medicines known to induce either CYP2C8 or CYP3A4(e.g. rifampicin, carbamazepine, phenytoin, efavirenz, nevirapine) is not recommended because efficacy may be compromised because of lower paclitaxel exposures.
This is becausethe drug is a stimulant and most drugs of this class are known to induce high blood pressure especially when abused.
Some chemotherapy is known to induce severe nausea and vomiting, and Akynzeo is used in patients receiving either highly emetogenic(vomit-inducing) chemotherapy based on the cancer medicine cisplatin, or other chemotherapies that are moderately emetogenic.
It safeguards your cells against damages caused by cost-free radicals andminimizes the secretion of estrogen that is known to induce weight gain.
Multiple shocks with a Taser have been known to induce ventricular fibrillation, which could cause cardiac arrest.
Special care is needed for those patients simultaneously starting treatment with Kivexa and other medicinal products known to induce skin toxicity(such as non-nucleoside reverse transcriptase inhibitors- NNRTIs).
The metabolism of bazedoxifene may be increased by concomitant use of substances known to induce UGTs, such as rifampicin, phenobarbital, carbamazepine, and phenytoin, potentially leading to decreased systemic concentrations of bazedoxifene.
Special care is needed for those patients simultaneously starting treatment with Ziagen and other medicinal products known to induce skin toxicity(such as non-nucleoside reverse transcriptase inhibitors- NNRTIs).
The metabolism of bazedoxifene may be increased by concomitant use of substances known to induce UGTs, such as rifampicin, phenobarbital, carbamazepine, and phenytoin, potentially leading to decreased systemic concentrations of bazedoxifene.
However no evidence of clinically significant adverse reactions was observed in the PLATO trial after concomitant administration with one ormore medicinal products known to induce bradycardia(e.g., 96% beta blockers, 33% calcium channel blockers diltiazem and verapamil, and 4% digoxin).
AIIRAs therapy exposure during the second and third trimesters is known to induce human fetotoxicity(decreased renal function, oligohydramnios, skull ossification retardation) and neonatal toxicity(renal failure, hypotension, hyperkalaemia).
However no evidence of clinically significant adverse reactions was observed in the PLATO trial after concomitant administration with one ormore medicinal products known to induce bradycardia(e.g., 96% beta blockers, 33% calcium channel blockers diltiazem and verapamil, and 4% digoxin)(see section 4.5).
AIIRAs therapy exposure during the second and third trimesters is known to induce human fetotoxicity(decreased renal function, oligohydramnios, skull ossification retardation) and neonatal toxicity(renal failure, hypotension, hyperkalaemia).
Particular caution must be used when prescribing Kaletra and medicinal products known to induce QT interval prolongation such as: chlorpheniramine, quinidine, erythromycin, clarithromycin.
ACE inhibitors therapy exposure during the second and third trimesters is known to induce human foetotoxicity(decreased renal function, oligohydramnios, skull ossification retardation) and neonatal toxicity(renal failure, hypotension, hyperkalaemia).
Particular caution must be used when prescribing Kaletra and medicinal products known to induce QT interval prolongation such as: chlorpheniramine, quinidine, erythromycin, clarithromycin.
Exposure to ARBs therapy during the second and third trimesters is known to induce human foetotoxicity(decreased renal function, oligohydramnios, skull ossification retardation) and neonatal toxicity(renal failure, hypotension, hyperkalaemia).
Exposure to AIIRA therapy during the second and third trimesters is known to induce human fetotoxicity(ecreased renal function, oligohydramnios, skull ossification retardation) and neonatal toxicity(r nal failure, hypotension, hyperkalaemia).(See section 5.3).
The metabolism of oestrogens may be increased by concomitant use of substances known to induce drug-metabolising enzymes, such as anticonvulsants(e.g., phenobarbital, phenytoin, carbamazepine) and anti-infectives(e.g., rifampicin, rifabutin, nevirapine, efavirenz).
The metabolism of oestrogens andprogestagens may be increased by concomitant use of substances known to induce drug-metabolising enzymes, specifically cytochrome P450 enzymes such as anticonvulsants(e.g. phenobarbital, phenytoin, carbamazepin) and anti-infectives(e.g. rifampicin, rifabutin, nevirapine, efavirenz).
Exposure to angiotensin II receptor antagonist therapy during the second and third trimesters is known to induce human fetotoxicity(decreased renal function, oligohydramnios, skull ossification retardation) and neonatal toxicity(renal failure, hypotension, hyperkalaemia)(see section 5.3).