Safety profile
The reassurance of treating your patients with the tried-and-trusted aflibercept molecule
In PULSAR and PHOTON, EYLEA 8mg demonstrated a safety profile consistent with EYLEA 2mg from baseline through Week 96:*

* EYLEA (aflibercept) 2mg was dosed at fixed Q8 intervals after 3 (nAMD) or 5 (DME) initial monthly injections.
PULSAR safety
Adverse events in patients receiving EYLEA 8mg were consistent with EYLEA 2mg
PULSAR: most frequent AEs through Week 48


Adapted from Korobelnik J-F. 2022.
* Any ocular treatment-emergent AE in the study eye.
† Treatment-emergent events.
‡ All events.
Abbreviations
2Q8, 2 mg every 8 weeks; 8Q12, 8 mg every 12 weeks; 8Q16, 8 mg every 16 weeks; AE, adverse event; APTC, Anti-Platelet Trialists’ Collaboration; DME, diabetic macular oedema; IOI, intraocular inflammation; IOP, intraocular pressure; MoA, mechanism of action; nAMD, neovascular (wet) age-related macular degeneration; Q8, every 8 weeks; SAE, serious adverse event; SAF, safety analysis set; TEAE, treatment-emergent adverse event.
PP-EYL_8mg-IE-0156-1 | January 2026
