Examples of using Repeat dose in English and their translations into Romanian
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In repeat dose studies in dogs, haemolytic anaemia was not observed.
No conventional acute and repeat dose toxicity studies were performed.
The repeat dose is not recommended in these populations.
The non clinical programme was based on 7 repeat dose toxicology studies in rats and dogs.
In repeat dose studies in dogs, haemolytic anaemia was not observed.
No hepatotoxicity was observed in rodents and monkeys in the repeat dose toxicity studies.
Single dose and repeat dose studies in a range of animal models(rats and primates) were performed.
No evidence of an associated risk was identified in the rat and monkey repeat dose toxicity studies.
Repeat dose toxicity studies longer than 5 days, reproductive toxicity studies and carcinogenicity studies.
Non-clinical data reveal no special hazard for humans based on repeat dose toxicity studies in monkeys.
Adverse reactions seen in repeat dose studies in animals include hyperpigmentation of the thyroid and tubular degeneration in the kidney.
Non-clinical data reveal no special hazard for humans based on conventional repeat dose toxicity and local tolerance studies.
Repeat dose toxicity studies in animals have shown that bevacizumab may have an adverse effect on female fertility(see section 5.3).
Ocular changes were inconsistently observed in repeat dose toxicity studies in rodents and dogs, but not in monkeys.
If a repeat dose is required to control the bleed, the prolonged half-life of ALPROLIX should be taken into account(see section 5.2).
Ocular changes were inconsistently observed in repeat dose toxicity studies in rodents and dogs, but not in monkeys.
Repeat dose toxicity studies with estradiol, nomegestrol acetate or combination have indicated expected estrogenic and gestagen effects.
The adjuvant, AF03,was not mutagenic or clastogenic and induced transient inflammatory changes in repeat dose toxicity studies(in rats and rabbits).
Repeat dose studies with fosamprenavir in rats produced effects consistent with hepatic enzyme induction, which predisposes rats to thyroid neoplasms.
Cataracts and lens opacities were observed in the repeat dose rodent toxicology and carcinogenicity studies, but were.
Non clinical data reveal no special hazards for humans based on conventional studies of safety pharmacology, repeat dose toxicity or genotoxicity.
Maximum doses in repeat dose toxicity studies were limited by the exaggerated pharmacologic effects of retigabine(including ataxia, hypokinesia and tremor).
Non-clinical studies demonstrated minor alterationsin liver enzymes and calcium levels in a repeat dose toxicity study in rats.
In repeat dose toxicity studies in mouse, rat, dog and the cynomolgus monkey main target organs of toxicity were the ovary, uterus and the liver.
Fertility studies with trabectedinwere not performed but limited histopathological changes were observed in the gonads in the repeat dose toxicity studies.
However, in repeat dose studies, testicular degeneration/depletion was seen in rats and dogs(≥0.2 times the human clinical exposure based on AUC).
Non-Clinical data obtained with Celvapan containing a H5N1 vaccine strain demonstrated alterations in liver enzymes andcalcium levels in repeat dose toxicity studies in rats.
Because of the design of the repeat dose toxicity studies and differences in pharmacokinetics in animals and humans, continuous exposure of animals was not assured in these studies.
Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology,single and repeat dose toxicity, genotoxicity, thrombogenicity and local tolerability.
A repeat dose toxicity study in rats, which included an evaluation of single-dose toxicity and local tolerance, revealed no special hazards to humans.