Aflibercept ophthalmic Side Effects
Medically reviewed by Drugs.com. Last updated on Aug 9, 2022.
More frequently reported side effects include: increased intraocular pressure. Continue reading for a comprehensive list of adverse effects.
Applies to aflibercept ophthalmic: intraocular solution.
Serious side effects
Along with its needed effects, aflibercept ophthalmic may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
Check with your doctor or nurse immediately if any of the following side effects occur while taking aflibercept ophthalmic:
- bloody eye
- blurred vision
- eye or eyelid redness
- eye pain
- seeing flashes, sparks of light, or a veil or curtain
- seeing floating spots before the eyes
- vision changes
- Bleeding or pain at the injection site
- swelling of the eyelid
- Fast heartbeat
- hives, itching, rash, or skin redness
- joint pain, stiffness, or swelling
- swelling of the eye, face, lips, hands, or feet
- tightness in the chest
- troubled breathing or swallowing
Incidence not known
- Pain in the chest, groin, or legs, especially the calves
- severe, sudden headache
- slurred speech
- sudden loss of coordination
- sudden, severe weakness or numbness in the arm or leg
Other side effects
Some side effects of aflibercept ophthalmic may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.
Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
- Feeling like something is in the eye
- watery eyes
For Healthcare Professionals
Applies to aflibercept ophthalmic: intravitreal solution.
Very common (10% or more): Conjunctival hemorrhage (28%), eye pain (13%),
Common (1% to 10%): Cataract, vitreous floaters, corneal erosion, intraocular pressure increased, conjunctival hyperemia, ocular hyperemia, vitreous detachment, foreign body sensation in eyes, lacrimation increased, vision blurred, intraocular inflammation, retinal pigment epithelium tear, injection site hemorrhage, eyelid edema, corneal edema, retinal degeneration, cataract, cataract nuclear, cataract subcapsular, corneal abrasion, intraocular pressure increased, vitreous floaters
Uncommon (0.1% to 1%): Retinal detachment, retinal tear, endophthalmitis injection site pain, traumatic cataract[Ref]
Common (1% to 10%): Injection site pain[Ref]
Intravitreal use of VEGF inhibitors has been associated with a potential risk of arterial thromboembolic events (ATEs) defined as nonfatal stroke, nonfatal myocardial infarction, or vascular death (including death of unknown cause). In wet age-related macular degeneration (AMD) studies, 1.8% (n=32/1824) and 1.5% (n=9/595) of patients treated with this drug or ranibizumab, respectively, experienced an ATE in the first 52 weeks and 3.3% and 3.2% through 96 weeks, respectively. In the diabetic macular edema (DME) studies, ATEs were reported at incidences of 3.3% (n=19/578) and 2.8% (n=8/287) through week 52, and 6.4% (n=37/578) and 4.2% (n=12/287) through week 100, in patients receiving 2 different dosing regimens of this drug or macular laser photocoagulation (after the first 24 weeks, all patients could receive drug or laser treatment). No ATEs have been reported in the first 6 months of the retinal vein occlusion (RVO) studies.[Ref]
Common (1% to 10%): Arterial thromboembolic events[Ref]
Uncommon (0.1% to 1%): Hypersensitivity
More about aflibercept ophthalmic
- Reviews (46)
- Dosage information
- During pregnancy
- Drug class: anti-angiogenic ophthalmic agents
- En español
Related treatment guides
1. Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0
2. Cerner Multum, Inc. "Australian Product Information." O 0
3. "Product Information. Eylea (aflibercept ophthalmic)." Regeneron Pharmaceuticals Inc (2011):
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Some side effects may not be reported. You may report them to the FDA.