Примери за използване на Trial data на Английски и техните преводи на Български
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in-vivo in numerous animal models, and has been confirmed by clinical trial data.
The frequency of all hypersensitivity reactions was estimated from clinical trial data as very common in CRF patients.
Dexrazoxane efficacy in the prevention of anthracycline cardiotoxicity is supported by available clinical trial data.
Table 2 Adverse drug reactions(ADRs) identified during post-marketing surveillance(frequencies- where known- calculated based on pooled clinical trial data N= 1,093).
Multiple Courses The limited clinical trial data on multiple courses of treatment of RA patients seem to be associated with a similar ADR profile to that observed following first exposure.
They need to start sharing clinical trial data, and in doing so,
Residue trial data shall be submitted in the Annex II dossier for those uses of plant protection products for which authorization is sought at the moment of introduction of a dossier for inclusion of the active substance in Annex I.
Adverse reactions listed below have been observed during clinical studies and/or during marketed use and are based on clinical trial data and classified according to MedDRA System Organ Class.
Although clinical trial data did not substantiate safety concerns raised from spontaneous ADR reporting,
In terms of safety, clinical trial data showed that the most commonly-reported adverse events are headaches,
Paediatric clinical trial data with vandetanib in MTC(see section 5.1)
Clinical trial data showed hypotension occurred in 7% of cinacalcet-treated patients,
Clinical trial data on incidence of new on-set HCC show higher point estimates for HCC after reaching SVR with IFN-free regimens compared to IFN-containing regimens,
since they had little to no chance of obtaining this clinical trial data from any court in the U.S.,
in HIV-1 protease were derived from clinical trial data of ART-experienced patients,
The review followed a previous assessment of clinical trial data which indicated that cases of blood clots
No person should be allowed to conduct trials in humans if a research project they are responsible for is currently withholding trial data from publication more than one year after completion.
This follows an initial assessment of clinical trial data with ponatinib, conducted in November 2013,
This follows an initial assessment of clinical trial data with Iclusig, conducted in November 2013,
the public easy access to clinical trial data,” Doshi reportedly stated in an email to CBC News.