Dictionary of Pharmaceutical Medicine by Dr. med. Dr. phil. Gerhard Nahler (auth.)

By Dr. med. Dr. phil. Gerhard Nahler (auth.)

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Distomer see CH IRALITY, ENANTI OME R. e. e. g. g. ) should be used. g . product analysis certificates inust also be considered. g. 3,5,7,9,12, 16 mg/m 2 ) ; generally about 3 subjects are treated at each non-toxic dose level; to avoid problems of eventual cumulative effects, subjects are usually exposed to not more than one dose level. g. e. decreasing with increasing doses; see also PHASE I. dosing schedule see TREAT MENT SCHEDULE. double blind see BLINDING . double data entry see DATA ENTRY.

G. ) should be used. g . product analysis certificates inust also be considered. g. 3,5,7,9,12, 16 mg/m 2 ) ; generally about 3 subjects are treated at each non-toxic dose level; to avoid problems of eventual cumulative effects, subjects are usually exposed to not more than one dose level. g. e. decreasing with increasing doses; see also PHASE I. dosing schedule see TREAT MENT SCHEDULE. double blind see BLINDING . double data entry see DATA ENTRY. o. g . tablets is increased, reducing COMPLIANCE of patients; see also BLINDING .

E. , one must be able to 23 co measure them; c. are not simply EFFECT MODIFIERS (which, in contrast, do not BIAS the overall estimate ofexposure-outcome associations) ; see also PLACEBO EFFECT, LEARNING EFFECT. consent see INFORMED CONSENT. g. Hungary; see also INFORMED CONSENT. consistency of data Degree of association among items, plausibility; examples for c. ; see also MEASUREMENT PROPERTIES. contingency table Tabulated DATA which are categorical, and mutually exclusive; entries into categories are actual numbers or counts.

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