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Altuvoct
Eintrag öffnenAltuvoct · 4.1 Therapeutic indications · 1
Eintrag öffnenAltuvoct · 4.3 Contraindications · 1
Eintrag öffnenAltuvoct · 4.3 · Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
Eintrag öffnenAltuvoct · 4.4 Special warnings and precautions for use · 1
Eintrag öffnenAltuvoct · 4.5 Interaction with other medicinal products and other forms of interaction · 1
Eintrag öffnenAltuvoct · 4.5 · No interaction studies have been performed.
Eintrag öffnenAltuvoct · 4.5 · No interactions of human coagulation factor VIII (rDNA) products with other medicinal products have been repor
Eintrag öffnenAltuvoct · 4.6 Fertility, pregnancy and lactation · 1
Eintrag öffnenAltuvoct · 4.8 Undesirable effects · 1
Eintrag öffnenAltuvoct · 4.8 · 7 Table 2: Adverse reactions reported for ALTUVOCT
Eintrag öffnenAltuvoct · 4.8 · Adverse drug reactions (ADRs) (summarized in Table 2) were reported in 111 (40.1%) of the 277 subjects treated
Eintrag öffnenAltuvoct · 4.8 · Development of neutralising antibodies (inhibitors) may occur in patients with haemophilia A treated with fact
Eintrag öffnenAltuvoct · 4.8 · Frequencies have been evaluated according to the following convention: very common (≥1/10); common (≥1/100 to
Eintrag öffnenAltuvoct · 4.8 · Hypersensitivity or allergic reactions (which may include angioedema, burning and stinging at the injection si
Eintrag öffnenAltuvoct · 4.8 · MedDRA system organ class Adverse reactions Frequency category 1 Blood and lymphatic system disorders Factor V
Eintrag öffnenAltuvoct · 4.8 · No age-specific differences in adverse reactions were observed between paediatric and adult patients.
Eintrag öffnenAltuvoct · 4.8 · Paediatric population
Eintrag öffnenAltuvoct · 4.8 · Reporting of suspected adverse reactions
Eintrag öffnenAltuvoct · 4.8 · Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows con
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