Примери за използване на Severity of adverse на Английски и техните преводи на Български
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nature and severity of adverse reactions did not differ between children and adults.
Frequency, type and severity of adverse reactions in children are expected to be the same as in all population groups except for the inhibitor formation.
type and severity of adverse reactions in children were found to be similar to those in adults.
as well as studying the impact and severity of adverse effects.
Prior treatment with other anti-inflammatory substances may result in additional or increased severity of adverse effects and accordingly a treatment-free period with such veterinary medicinal products should be observed before the commencement of treatment with this veterinary medicinal product.
Prior treatment with other anti-inflammatory substances may result in additional or increased severity of adverse effects and accordingly a treatment-free period with such drugs should be observed before the commencement of treatment with this veterinary medicinal product.
increased number or severity of adverse events.
Two doses up to 20 mg/kg administered 21 days apart by intravenous infusion have been given to humans with no increase in incidence or severity of adverse reactions compared with doses of 1, 4, or 10 mg/kg.
Severity of adverse reaction.
Generally, an increased frequency and higher severity of adverse reactions may result from overdose.
The occurrence and severity of adverse reactions depend on dosage level
The type and severity of adverse reactions in subjects with cirrhosis were overall comparable to those seen in subjects without cirrhosis.
type and severity of adverse reactions in paediatric patients were comparable to those observed in adults.
Frequency, type and severity of adverse reactions in children are expected to be the same as in adults(see section 5.1).
the type and severity of adverse reactions associated with each of the compounds may be expected.
The frequency, type and severity of adverse reactions in the adolescent population were observed to be similar to those seen in adults.
they cannot measure the probability or severity of adverse events.
Overall the frequency, type and severity of adverse reactions in the paediatric population do not indicate differences to the experience in the adult population.
the type and severity of adverse reactions associated with each of the compounds may be expected.
the type and severity of adverse reactions associated with each of these components may be expected in the combination.