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CoAprovel · 4.8 · 41 experienced adverse reactions. The most commonly reported ADRs were dizziness (5.6%), fatigue (4.9%), nause
Eintrag öffnenCoAprovel · 4.8 · 58 experienced adverse reactions. The most commonly reported ADRs were dizziness (5.6%), fatigue (4.9%), nause
Eintrag öffnenCoAprovel · 4.8 · 75 experienced adverse reactions. The most commonly reported ADRs were dizziness (5.6%), fatigue (4.9%), nause
Eintrag öffnenCotellic · 4.8 · 11 Table 3 Adverse drug reactions (ADRs) in patients treated with Cotellic in combination with vemurafenib in
Eintrag öffnenCotellic · 4.8 · ADRs which were reported in melanoma patients are listed below by MedDRA body system organ class, frequency an
Eintrag öffnenCotellic · 4.8 · Adverse drug reactions (ADRs) are based on results from a multi-centre, randomised, double-blind, placebo-cont
Eintrag öffnenCyramza · 4.8 · 12 Within each frequency grouping, ADRs are presented in order of decreasing seriousness.
Eintrag öffnenCyramza · 4.8 · 13 Table 7: ADRs reported in patients treated with ramucirumab in combination with chemotherapy or erlotinib i
Eintrag öffnenCyramza · 4.8 · Table 6: ADRs reported in patients treated with ramucirumab as monotherapy in phase 3 clinical trials (REGARD,
Eintrag öffnenCyramza · 4.8 · Table 8: ADRs associated with ramucirumab reported in clinical trials and through post- marketing reporting
Eintrag öffnenCyramza · 4.8 · Tables 6 and 7 below list the adverse drug reactions (ADRs) from placebo controlled phase III clinical trials
Eintrag öffnenDovprela (previously Pretomanid FGK) · 4.8 · 7 ADRs attributed to moxifloxacin are marked with §.
Eintrag öffnenDovprela (previously Pretomanid FGK) · 4.8 · 9 Δ: ADRs that are attributed to linezolid. §: ADRs that are attributed to Moxifloxacin
Eintrag öffnenDovprela (previously Pretomanid FGK) · 4.8 · In the TB-PRACTECAL trial in which moxifloxacin was administered along with BPaL regimen, ADRs of increased tr
Eintrag öffnenDovprela (previously Pretomanid FGK) · 4.8 · In the TB-PRACTECAL trial, 52 patients reported ADRs of myelosuppression in the BPaLM arm, out of which 27 (18
Eintrag öffnenDovprela (previously Pretomanid FGK) · 4.8 · The most frequent adverse drug reactions (ADRs) during treatment with pretomanid in combination with bedaquili
Eintrag öffnenDovprela (previously Pretomanid FGK) · 4.8 · The table below displays ADRs, by system organ class and frequency, which are considered at least possibly rel
Eintrag öffnenEdurant · 4.8 · 33 in the rilpivirine arm and efavirenz arm was 104.3 and 104.1 weeks, respectively. Most ADRs occurred in the
Eintrag öffnenEdurant · 4.8 · ADRs reported in adult patients treated with rilpivirine are summarised in Table 2. The ADRs are listed by sys
Eintrag öffnenEdurant · 4.8 · ADRs reported in adult patients treated with rilpivirine are summarised in Table 3. The ADRs are listed by sys
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