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dlhodobé štúdie kancerogenity neboli vykonané.
long-term carcinogenicity studies have not been carried out.
Last Update: 2017-04-26
Usage Frequency: 3
Quality:
s kyselinou karglumovou sa neuskutočnili žiadne štúdie kancerogenity.
no carcinogenicity study has been conducted with carglumic acid.
Last Update: 2017-04-26
Usage Frequency: 3
Quality:
v štúdii kancerogenity u potkanov leflunomid nepreukázal kancerogénny potenciál.
in a carcinogenicity study in rats, leflunomide did not show carcinogenic potential.
Last Update: 2017-04-26
Usage Frequency: 3
Quality:
s dihydrátom octanu zinočnatého neboli robené žiadne konvenčné štúdie kancerogenity.
no conventional carcinogenicity study has been conducted with zinc acetate dihydrate.
Last Update: 2017-04-26
Usage Frequency: 3
Quality:
Štandardné štúdie dlhodobej toxicity, reprodukcie, mutagenity a kancerogenity boli uskutočnené na
higher blood levels may be associated with increased incidence of nausea and vomiting.
Last Update: 2012-04-12
Usage Frequency: 2
Quality:
Štandardné štúdie dlhodobej toxicity, reprodukcie, mutagenity a kancerogenity boli uskutočnené na laboratórnych zvieratách.
conventional long-term toxicity, reproduction, mutagenicity, and carcinogenicity studies have been performed in laboratory animals.
Last Update: 2017-04-26
Usage Frequency: 1
Quality:
v štúdii kancerogenity u myší sa vyskytli v skupine s najvyššími dávkami malígne lymfómy u samcov, čo sa pripisuje imunosupresívnemu účinku leflunomidu.
in a carcinogenicity study in mice an increased incidence of malignant lymphoma occurred in males of the highest dose group, considered to be due to the immunosuppressive activity of leflunomide.
Last Update: 2017-04-26
Usage Frequency: 3
Quality:
v štúdiách dermálnej kancerogenity u myší trvajúcej 24 mesiacov, ktorým sa aplikovala 0,1% masť, sa nevyskytli žiadne kožné tumory.
in a 24-month dermal carcinogenicity study performed in mice with 0.1% ointment, no skin tumours were observed.
Last Update: 2017-04-26
Usage Frequency: 3
Quality:
v štúdiách na sledovanie systémovej kancerogenity u myší (18 mesiacov) a potkanov (24 mesiacov) sa nedokázal kancerogénny potenciál takrolimu.
systemic carcinogenicity studies in mice (18 months) and rats (24 months) revealed no carcinogenic potential of tacrolimus.
Last Update: 2017-04-26
Usage Frequency: 1
Quality:
kancerogenita v štúdiách na sledovanie systémovej kancerogenity u myší (18 mesiacov) a potkanov (24 mesiacov) sa nedokázal kancerogénny potenciál takrolimu.
carcinogenicity systemic carcinogenicity studies in mice (18 months) and rats (24 months) revealed no carcinogenic potential of tacrolimus.
Last Update: 2011-10-23
Usage Frequency: 1
Quality:
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Štúdie kancerogenity u potkanov nepreukázali žiadny onkogénny potenciál, zatiaľ čo zvýšený výskyt hepatocelulárnych nádorov u samcov myší je považovaný za dôsledok známeho negenotoxického fenoménu, známeho u hlodavcov, ktorého mechanizmus účinku sa vzťahuje k indukcii pečeňových enzýmov, podobnej ako po fenobarbitále.
carcinogenicity studies did not indicate any oncogenic potential in rats, whereas increased incidences of hepatocellular tumors in male mice are considered to result of a non-genotoxic, mode of action linked to a phenobarbitone- like liver enzyme induction, which is a known rodent specific phenomenon.
Last Update: 2017-04-26
Usage Frequency: 1
Quality: