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adverse reactions were experienced by 2,256 (32.2%) of the patients treated with edoxaban 60 mg (30 mg dose reduced) in the engage af-timi 48 study and 1,249 (30.3%) in the hokusai-vte study.
kõrvaltoimeid tekkis uuringus engage af-timi 48 kokku 2256 (32,2%) patsiendil, keda raviti edoksabaani 60 mg-ga (vähendatud annusega 30 mg), ja uuringus hokusai-vte kokku 1249 (30,3%) patsiendil.