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Beovu · 4.8 · Reporting of suspected adverse reactions
Eintrag öffnenBeovu · 4.8 · Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows con
Eintrag öffnenBeovu · 4.8 · Summary of the safety profile
Eintrag öffnenBeovu · 4.8 · Table 1 Frequencies of adverse reactions in clinical studies
Eintrag öffnenBeovu · 4.8 · Tabulated list of adverse reactions
Eintrag öffnenBeovu · 4.8 · The adverse reactions experienced following administration of Beovu in clinical studies are summarised in Tabl
Eintrag öffnenBeovu · 4.8 · The most frequently reported adverse reactions were cataract (9.0%), conjunctival haemorrhage (6.5%) and intra
Eintrag öffnenBeovu · 4.8 · The most frequently reported adverse reactions were reduced visual acuity (7.3%), cataract (7.0%), conjunctiva
Eintrag öffnenBeovu · 4.8 · The most serious adverse reactions were blindness (0.8%), endophthalmitis (0.7%), retinal artery occlusion (0.
Eintrag öffnenBeovu · 4.8 · The most serious adverse reactions were cataract (9.0%), retinal vascular occlusion (1.1%), retinal artery occ
Eintrag öffnenBeovu · 4.8 · Wet AMD After dosing with Beovu for 88 weeks, treatment-emergent anti-brolucizumab antibodies were detected in
Eintrag öffnenBeovu · 4.8 · Wet AMD For wet AMD, a total of 1 088 patients treated with brolucizumab constituted the safety population in
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