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Beovu
Eintrag öffnenBeovu · 4.1 Therapeutic indications · 1
Eintrag öffnenBeovu · 4.3 Contraindications · 1
Eintrag öffnenBeovu · 4.3 · Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
Eintrag öffnenBeovu · 4.3 · Patients with active intraocular inflammation.
Eintrag öffnenBeovu · 4.3 · Patients with active or suspected ocular or periocular infections.
Eintrag öffnenBeovu · 4.4 Special warnings and precautions for use · 1
Eintrag öffnenBeovu · 4.5 Interaction with other medicinal products and other forms of interaction · 1
Eintrag öffnenBeovu · 4.5 · No interaction studies have been performed.
Eintrag öffnenBeovu · 4.6 Fertility, pregnancy and lactation · 1
Eintrag öffnenBeovu · 4.8 Undesirable effects · 1
Eintrag öffnenBeovu · 4.8 · 8 Intraocular pressure increase Common Conjunctivitis Common Retinal pigment epithelial tear Common Vision blu
Eintrag öffnenBeovu · 4.8 · Adverse reactions (Table 1) are listed according to the MedDRA system organ class. Within each system organ cl
Eintrag öffnenBeovu · 4.8 · Among AMD and DME patients with treatment-emergent antibodies, a higher number of intraocular inflammation adv
Eintrag öffnenBeovu · 4.8 · DME After dosing with Beovu for 96 weeks, treatment-emergent anti-brolucizumab antibodies were detected in 16-
Eintrag öffnenBeovu · 4.8 · DME For DME, a total of 558 patients treated with brolucizumab constituted the safety population in two Phase
Eintrag öffnenBeovu · 4.8 · Description of selected adverse reactions
Eintrag öffnenBeovu · 4.8 · Immunogenicity There is a potential for an immune response in patients treated with Beovu.
Eintrag öffnenBeovu · 4.8 · MedDRA System organ class Frequency category* Immune system disorders Hypersensitivity (including urticaria, r
Eintrag öffnenBeovu · 4.8 · Product-class-related adverse reactions There is a theoretical risk of arterial thromboembolic events, includi
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