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Abilify · 4.8 · Tabulated list of adverse reactions
Eintrag öffnenAbilify · 4.8 · Tabulated list of adverse reactions
Eintrag öffnenAbilify · 4.8 · The following adverse reactions had a possible dose response relationship; extrapyramidal disorder (incidences
Eintrag öffnenAbilify · 4.8 · The following adverse reactions had a possible dose response relationship; extrapyramidal disorder (incidences
Eintrag öffnenAbilify · 4.8 · The following adverse reactions had a possible dose response relationship; extrapyramidal disorder (incidences
Eintrag öffnenAbilify · 4.8 · The frequency of adverse reactions reported during post-marketing use cannot be determined as they are derived
Eintrag öffnenAbilify · 4.8 · The frequency of adverse reactions reported during post-marketing use cannot be determined as they are derived
Eintrag öffnenAbilify · 4.8 · The frequency of adverse reactions reported during post-marketing use cannot be determined as they are derived
Eintrag öffnenAbilify · 4.8 · The frequency of adverse reactions reported during post-marketing use cannot be determined as they are derived
Eintrag öffnenAbilify · 4.8 · The incidences of the Adverse Drug Reactions (ADRs) associated with aripiprazole therapy are tabulated below.
Eintrag öffnenAbilify · 4.8 · The incidences of the Adverse Drug Reactions (ADRs) associated with aripiprazole therapy are tabulated below.
Eintrag öffnenAbilify · 4.8 · The incidences of the Adverse Drug Reactions (ADRs) associated with aripiprazole therapy are tabulated below.
Eintrag öffnenAbilify · 4.8 · The most commonly reported adverse reactions in placebo-controlled trials were akathisia and nausea each occur
Eintrag öffnenAbilify · 4.8 · The most commonly reported adverse reactions in placebo-controlled trials were akathisia and nausea each occur
Eintrag öffnenAbilify · 4.8 · The most commonly reported adverse reactions in placebo-controlled trials were akathisia and nausea each occur
Eintrag öffnenAbilify · 4.8 · The most commonly reported adverse reactions in placebo-controlled trials were nausea, dizziness and somnolenc
Eintrag öffnenAbiraterone Accord · 4.8 · 8 The following CTCAE (version 4.0) Grade 3 adverse reactions occurred in patients treated with abiraterone ac
Eintrag öffnenAbiraterone Accord · 4.8 · Adverse reactions observed during clinical studies and post-marketing experience are listed below by frequency
Eintrag öffnenAbiraterone Accord · 4.8 · Adverse reactions observed during clinical studies and post-marketing experience are listed below by frequency
Eintrag öffnenAbiraterone Accord · 4.8 · Description of selected adverse reactions Cardiovascular reactions The three Phase 3 studies excluded patients
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