Voorbeelden van het gebruik van Repeated dose in het Engels en hun vertalingen in het Nederlands
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Non-clinical data reveal no special hazard for humans based on studies of single dose toxicity, repeated dose toxicity, and genotoxicity.
In repeated dose toxicity studies in rats
In humans, piperaquine has a Tmax of approximately 5 hours following a single and repeated dose.
Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, repeated dose toxicity, toxicity to reproduction and development.
If there is no effect after a repeated dose, they switch to stronger drugs with a positive chronotropic effect.
Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, repeated dose toxicity, and genotoxicity.
No special hazard for humans was identified based on conventional studies of single and repeated dose toxicity and genotoxicity.
naloxone has been investigated in acute and repeated dose(up to 90 days in rats) toxicity studies in animals.
Nilotinib has been evaluated in safety pharmacology, repeated dose toxicity, genotoxicity, reproductive toxicity and phototoxicity studies.
Also, it is desirable that one of the species is the same as in the repeated dose toxicity studies.
of that study or in the 13 weeks repeated dose toxicity study in rats without recovery.
Whenever more than one batch of active substance is used in repeated dose toxicity studies this must be stated and each batch identified.
dog whether administered as single dose or as repeated dose.
an overdose and a repeated dose regimen.
Bosutinib has been evaluated in safety pharmacology, repeated dose toxicity, genotoxicity, reproductive toxicity and photoxicity studies.
The major observed effects in the repeated dose toxicity studies were those related to the pharmacodynamic action of apixaban on blood coagulation parameters.
Preclinical data including single-dose, repeated dose and local tolerance studies revealed no unexpected findings
Comparison of the single and repeated dose studies revealed that toxicity was related primarily to duration of exposure.
As rodents do not react to human interferon beta, repeated dose studies were carried out with rhesus monkeys.
In a 14-day repeated dose study, AUC increased 3-fold from Day 1to Day 14.