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Combivir · 4.8 · The adverse reactions considered at least possibly related to the treatment are listed below by body system, o
Eintrag öffnenComirnaty · 4.8 · Infants 6 months to 23 months of age - after at least 3 doses In 3 groups from Study 6 (Phase 1), 95 participa
Eintrag öffnenComirnaty · 4.8 · Infants 6 months to 23 months of age - after at least 3 doses In 3 groups from Study 6 (Phase 1), 95 participa
Eintrag öffnenComirnaty · 4.8 · Infants 6 months to 23 months of age - after at least 3 doses In 3 groups from Study 6 (Phase 1), 95 participa
Eintrag öffnenComirnaty · 4.8 · Infants 6 months to 23 months of age - after at least 3 doses In 3 groups from Study 6 (Phase 1), 95 participa
Eintrag öffnenComirnaty · 4.8 · Infants 6 months to 23 months of age - after at least 3 doses In 3 groups from Study 6 (Phase 1), 95 participa
Eintrag öffnenCresemba · 4.8 · The clinical safety of isavuconazole was assessed in 77 paediatric patients who received at least one dose of
Eintrag öffnenCresemba · 4.8 · The clinical safety of isavuconazole was assessed in 77 paediatric patients who received at least one dose of
Eintrag öffnenDapagliflozin Viatris · 4.8 · rate. * Reported in ≥ 2% of subjects and ≥ 1% more and at least 3 more subjects treated with dapagliflozin 10
Eintrag öffnenDapagliflozin Viatris · 4.8 · subjects and ≥ 0.1% more and at least 3 more subjects treated with dapagliflozin 10 mg compared to placebo.
Eintrag öffnenDarunavir Viatris (previously Darunavir Mylan) · 4.8 · ● 80 ART-experienced HIV-1 infected paediatric patients aged from 6 to 17 years and weighing at least 20 kg wh
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 · 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 öffnenEfavirenz Teva · 4.8 · Adverse reactions of moderate or greater severity with at least possible relationship to treatment regimen (ba
Eintrag öffnenEiyzey · 4.8 · The most frequently observed adverse reactions (in at least 5% of patients treated with aflibercept) were conj
Eintrag öffnenEiyzey · 4.8 · The most frequently observed adverse reactions (in at least 5% of patients treated with aflibercept) were conj
Eintrag öffnenElaprase · 4.8 · 6 also tested positive for neutralizing antibodies on at least 3 consecutive study visits. Antibody-negative p
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