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We evaluated concomitant medication usage during the first 6 months of the prospective, observational, European Schizophrenia Outpatient Health Outcomes (SOHO) study, examining its frequency, variation according to type of antipsychotic drug used, and impact on treatment tolerability.
There was no difference in the presence or absence of MAP DNA when analysed according to disease activity and/or concomitant medication usage at the time of phlebotomy (Figure 7).
Concomitant medication usage was consistent with the primary diagnoses.
Summary statistics for efficacy endpoints were reported by treatment and concomitant medication usage status.
During each study visit, clinical events, study drug compliance and concomitant medication usage are documented.
Concomitant medication usage was equally distributed across the treatment groups and was in line with recommendations at the time the study was conducted.
Similar(51)
These findings were consistent despite variations in geographic area, dosage of EPA or DHA or concomitant medication use.
Concomitant medication use was similar across groups.
Concomitant medication use could have influenced ST levels.
Concomitant medication use was similar between CD types.
The number of concomitant medications and usage of specific medications at baseline were not significant predictors of progression in IADL in the multivariate mixed-effects models in the current study, suggesting that comorbidity did not influence the functional outcome.
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