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Tenkasi (previously Orbactiv) · 4.8 · Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows con
Eintrag öffnenTenkasi (previously Orbactiv) · 4.8 · Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows con
Eintrag öffnenTenkasi (previously Orbactiv) · 4.8 · Summary of the safety profile
Eintrag öffnenTenkasi (previously Orbactiv) · 4.8 · Summary of the safety profile
Eintrag öffnenTenkasi (previously Orbactiv) · 4.8 · Table 2: Frequency of adverse reactions by system organ class System organ class Frequency Adverse Reactions I
Eintrag öffnenTenkasi (previously Orbactiv) · 4.8 · Table 3: Frequency of adverse reactions by system organ class System organ class Frequency Adverse Reactions I
Eintrag öffnenTenkasi (previously Orbactiv) · 4.8 · Tabulated list of adverse reactions
Eintrag öffnenTenkasi (previously Orbactiv) · 4.8 · Tabulated list of adverse reactions
Eintrag öffnenTenkasi (previously Orbactiv) · 4.8 · The most commonly reported adverse reactions (≥5%) were: nausea, hypersensitivity reactions, infusion site rea
Eintrag öffnenTenkasi (previously Orbactiv) · 4.8 · The most commonly reported adverse reactions (≥5%) were: nausea, hypersensitivity reactions, infusion site rea
Eintrag öffnenTenkasi (previously Orbactiv) · 4.8 · The safety assessment in paediatric patients is based on data from one trial in which 38 patients aged from 3
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