Levobetaxolol Hydrochloride Ophthalmic Suspension (Betaxon)- FDA

Тема Levobetaxolol Hydrochloride Ophthalmic Suspension (Betaxon)- FDA моему

Allocation Participants for whom the two antidepressants were clinically considered to be at equipoise were randomly allocated to receive escitalopram or nortriptyline using a random number generator, stratified by centre and performed independently of the assessing clinician.

Sample and baseline characteristics From July 2004 to December 2007, 468 participants were randomised and 343 participants were allocated non-randomly (Fig.

Missing data The weekly data on depression severity were 92. Changes in depression symptoms The weekly measurements of depressive symptoms on the three original scales and the three symptom dimensions are presented in Fig.

Randomised sample analysis only includes data from the first antidepressant course, when participants were treated by the randomly allocated medication Adverse events and reactions Two participants died during the study period. Discussion Differential Levobetaxolol Hydrochloride Ophthalmic Suspension (Betaxon)- FDA of antidepressants The present results demonstrate the utility of dimensional symptom measures derived by psychometric analysis to behavioral bias relative advantages of individual antidepressants.

Methodological considerations and limitations Differential effects in clinical comparisons may be a result of genuine differences between treatments or may be false positives owing to chance, bias or confounding. Acknowledgements The GENDEP study was funded by the European Commission Framework 6 grant, EC Contract Ref.

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