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Joenja · 4.8 Undesirable effects · 1
Eintrag öffnenJoenja · 4.8 · 6 System organ class Adverse reaction Frequency General disorders and administration Fatigue Common site condi
Eintrag öffnenJoenja · 4.8 · Description of selected adverse reactions
Eintrag öffnenJoenja · 4.8 · Hypersensitivity Hypersensitivity reactions have been identified during post-marketing use of Joenja.
Eintrag öffnenJoenja · 4.8 · Neutrophil count decreased Seven (33%) patients receiving leniolisib developed a transient absolute neutrophil
Eintrag öffnenJoenja · 4.8 · Paediatric population
Eintrag öffnenJoenja · 4.8 · Reporting of suspected adverse reactions
Eintrag öffnenJoenja · 4.8 · Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows con
Eintrag öffnenJoenja · 4.8 · Summary of safety profile
Eintrag öffnenJoenja · 4.8 · Table 1 Adverse reactions System organ class Adverse reaction Frequency Immune system disorders Hypersensitivi
Eintrag öffnenJoenja · 4.8 · Tabulated list of adverse reactions
Eintrag öffnenJoenja · 4.8 · The following list of adverse reactions is based on experience from clinical trials and on postmarketing exper
Eintrag öffnenJoenja · 4.8 · The most commonly reported adverse reactions during leniolisib treatment were headache (32%), vomiting (16%),
Eintrag öffnenJoenja · 4.8 · The safety of leniolisib was evaluated in 38 adolescent and adult patients with APDS who participated in the p
Eintrag öffnenJoenja · 4.8 · Thirteen patients aged 12 to 17 were treated with leniolisib in the clinical trials. Frequency, type, and seve
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