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no patients discontinued from the study due to a teae in the sbr arm.
sbr lietotāju grupā teae dēļ no pētījuma neizstājās neviens pacients.
Last Update: 2017-04-26
Usage Frequency: 1
Quality:
the incidence of subjects with at least 1 treatment-emergent adverse event (teae) was similar between the resolor treatment group (69.8%) and the placebo treatment group (60.7%).
pacientu gadījumu skaits vismaz ar 1 ārstēšanas izraisītu blakusparādību resolor terapijas grupai (69,8%) un placebo terapijas grupai (60,7%) bija līdzīgs.
Last Update: 2017-04-26
Usage Frequency: 1
Quality:
