Exemple de utilizare a Teratogenicity în Engleză și traducerile lor în Română
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Impairment of fertility and teratogenicity.
Teratogenicity was not observed in rats or rabbits.
There is no evidence of its embryotoxicity or teratogenicity.
Teratogenicity and the need to avoid foetal exposure.
Studies in animals have shown teratogenicity(see section 5.3).
Teratogenicity is a suspected class effect of ERAs.
There was no evidence of teratogenicity in rats or rabbits.
Animal studies have not shown any evidence of foetotoxicity or teratogenicity.
There was no teratogenicity with rilpivirine in rats and rabbits.
Artenimol causes embryolethality and teratogenicity in rats and rabbits.
There was no teratogenicity with rilpivirine in rats and rabbits.
Prenatal developmental toxicity study(teratogenicity study).
The risk of teratogenicity and relevant risk minimisation advice.
The capsules must not be opened due to risk of teratogenicity(see section 5.3).
There was no evidence of teratogenicity in rats or rabbits treated with the losartan/ hydrochlorothiazide combination.
Studies in animals have shown embryotoxicity and teratogenicity(see section 5.3).
Teratogenicity could not be assessed at higher parenteral doses in rabbits as they induced maternal toxicity and abortion.
In rabbits, when administered prior to mating, teratogenicity has been observed.
Teratogenicity was noted in rabbits given 1000 mg/kg/day(15 times the exposure from the recommended human dose on an AUC basis).
There was no effect on foetal development and no evidence of teratogenicity.
The risk of anaemia, hepatotoxicity and teratogenicity and the need for reliable contraception;
Higher doses resulted in maternal andfoetal toxicity without evidence of teratogenicity.
Background information on mycophenolate mofetil teratogenicity and mutagenicity in humans.
Contraindication in pregnancy and in breast-feeding women due to potential teratogenicity.
No evidence of embryo-foetal toxicity or teratogenicity was observed in rats treated with sacubitril.
Higher doses resulted in maternal andfoetal toxicity without evidence of teratogenicity.
In embryotoxicity and teratogenicity studies in mice, dose-related increases in foetal resorption and teratogenicity were observed.
Studies in animals have shown reproductive toxicity,including teratogenicity.
Animal studies have shown no evidence of teratogenicity but embryolethality was seen in both rat and rabbit studies(see section 5.3).
Aliskiren was devoid of any mutagenic potential,embryo-foetal toxicity or teratogenicity.