Bevacizumab (Intravitreal)
Brand names: Avastin (off-label intravitreal)
Intravitreal bevacizumab is a recombinant humanised anti-VEGF monoclonal antibody used off-label by ophthalmologists to treat neovascular (wet) age-related macular degeneration, diabetic macular oedema and other retinal vascular disorders. It is administered as a direct injection into the vitreous cavity.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
Clinical monograph
How it works
It binds and neutralises all isoforms of vascular endothelial growth factor A, suppressing the abnormal choroidal and retinal neovascularisation and vascular leakage that cause macular oedema and visual loss.
Prescribing in practice
- Strict aseptic intravitreal injection technique is essential, as endophthalmitis is a sight-threatening complication; warn the patient to report increasing pain, redness or visual loss urgently.
- Use in the eye is off-label (the licensed indication is oncology), so local governance, informed consent and compounding from a quality-assured source are required.
- Avoid in active ocular or periocular infection and counsel that a transient rise in intraocular pressure can follow injection.
Monitoring
Monitor intraocular pressure and optic nerve perfusion around the time of injection and review retinal status with optical coherence tomography and visual acuity at each follow-up.
Counselling the patient
- Report any eye pain, worsening redness, light sensitivity or sudden drop in vision after injection without delay.
- Floaters and mild irritation are common in the first day or two and usually settle.
- Attend all scheduled review and re-treatment appointments to protect your vision.
Evidence & guidelines
Comparative trials such as CATT and IVAN found intravitreal bevacizumab non-inferior to ranibizumab for visual acuity in neovascular AMD, supporting its widespread off-label use.
Reference: CATT Trial (NEJM 2011); IVAN Trial (Lancet 2013); RCOphth AMD Guidelines; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- SMART Risk Score for Recurrent CVD · Cardiovascular Risk
- PCSK9 Inhibitor Eligibility Assessment · Lipid Management
- Insulin Correction Factor (ICF/ISF) · Insulin Management
- R Factor for Drug-Induced Liver Injury (DILI) · Liver Disease
- Revised Original International Autoimmune Hepatitis Score (IAIHG) · Autoimmune Liver Disease
- Immune-Related Adverse Events (irAE) -- GI Toxicity Colitis Grading · Oncology-Related GI
- Acute Red Eye / Vision Loss Screen · RCOphth 2020; NICE CKS
- Idiopathic Intracranial Hypertension · ABN; consensus 2018
- Acute Red Eye Assessment · RCOphth / AAO
- Acute Angle Closure Glaucoma · RCOphth / EGS Guidelines
- Retinal Detachment · RCOphth Guidelines / EURETINA
- Diabetic Retinopathy — Screening and Management · NICE NG28 2016 / NHS DES Programme