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Edurant · 4.8 · All ADRs were mild or moderate. ADRs reported in at least 2 participants, regardless of severity, were: decrea
Eintrag öffnenEdurant · 4.8 · All ADRs were mild or moderate. ADRs reported in at least 2 participants, regardless of severity, were: decrea
Eintrag öffnenEdurant · 4.8 · All ADRs were mild or moderate. ADRs reported in at least 2 participants, regardless of severity, were: vomiti
Eintrag öffnenEdurant · 4.8 · All ADRs were mild or moderate. ADRs reported in at least 2 participants, regardless of severity, were: vomiti
Eintrag öffnenEdurant · 4.8 · Most ADRs were grade 1 or 2. The most common ADRs reported in Study TMC278-C213 Cohort 1 (all grades, greater
Eintrag öffnenEdurant · 4.8 · Most ADRs were grade 1 or 2. The most common ADRs reported in Study TMC278-C213 Cohort 1 (all grades, greater
Eintrag öffnenEdurant · 4.8 · Selected treatment-emergent clinical laboratory abnormalities (grade 3 or grade 4), considered as ADRs, report
Eintrag öffnenEdurant · 4.8 · Selected treatment-emergent clinical laboratory abnormalities (grade 3 or grade 4), considered as ADRs, report
Eintrag öffnenEdurant · 4.8 · Table 2: ADRs reported in antiretroviral treatment-naïve HIV-1 infected adult patients treated with Rilpivirin
Eintrag öffnenEdurant · 4.8 · Table 3: ADRs reported in antiretroviral treatment-naïve HIV-1 infected adult patients treated with Rilpivirin
Eintrag öffnenEmblaveo · 4.8 · The ADRs listed in the table below are presented by System Organ Class (SOC) and frequency categories, defined
Eintrag öffnenEmblaveo · 4.8 · The following ADRs have been reported with aztreonam alone and/or identified during Phase 2 and Phase 3 clinic
Eintrag öffnenEmblaveo · 4.8 · The most common adverse drug reactions (ADRs) in patients treated with aztreonam/avibactam (ATM-AVI) were anae
Eintrag öffnenErivedge · 4.8 · 8 Table 1 ADRs occurring in patients treated with Erivedge
Eintrag öffnenErivedge · 4.8 · Tabulated list of adverse reactions ADRs are presented in table 1 below by system organ class (SOC) and absolu
Eintrag öffnenEurartesim · 4.8 · Description of selected adverse reactions The ADRs noted for Eurartesim were generally mild in severity, and t
Eintrag öffnenEurartesim · 4.8 · Description of selected adverse reactions The ADRs noted for Eurartesim were generally mild in severity, and t
Eintrag öffnenEurartesim · 4.8 · Frequency of ADRs in adult patients participating in clinical studies with Eurartesim and post- marketing data
Eintrag öffnenEurartesim · 4.8 · Frequency of ADRs in adult patients participating in clinical studies with Eurartesim and post- marketing data
Eintrag öffnenEurartesim · 4.8 · Frequency of ADRs in paediatric patients participating in clinical studies with Eurartesim and post- marketing
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