Faricimab (Intravitreal)
Brand names: Vabysmo
Faricimab is a bispecific monoclonal antibody given by intravitreal injection for neovascular (wet) age-related macular degeneration and diabetic macular oedema.
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 simultaneously binds and neutralises both vascular endothelial growth factor-A and angiopoietin-2, reducing vascular leakage, neovascularisation and inflammation, and helping stabilise the retinal vasculature.
Prescribing in practice
- Intravitreal injection carries a risk of endophthalmitis and intraocular inflammation, so it must be given under aseptic conditions and patients told to report eye pain, redness or worsening vision urgently.
- It is contraindicated in active or suspected ocular or periocular infection and active intraocular inflammation.
- A transient rise in intraocular pressure can occur after injection, so perfusion of the optic nerve head and pressure should be assessed.
Monitoring
Assess intraocular pressure and optic nerve perfusion around the time of injection and review visual acuity and retinal imaging to guide the treatment interval.
Counselling the patient
- Report eye pain, increasing redness, light sensitivity, floaters or any drop in vision without delay, as these can signal infection.
- Mild eye irritation or a small bleed on the white of the eye after the injection is common and usually settles.
- Attend all follow-up appointments, as injections are given on a planned and sometimes extending schedule.
Evidence & guidelines
The TENAYA, LUCERNE, YOSEMITE and RHINE trials demonstrated non-inferior visual outcomes with faricimab and the potential for extended dosing intervals in wet AMD and diabetic macular oedema.
Reference: NICE TA924; TENAYA/LUCERNE Trials (Lancet 2022); YOSEMITE/RHINE Trials; SPC Vabysmo; 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.
- Revised Original International Autoimmune Hepatitis Score (IAIHG) · Autoimmune Liver Disease
- Ho Index for Predicting Response to Medical Therapy in IBD · Inflammatory Bowel Disease
- Rh(D) Immune Globulin Dosage for Maternal-Fetal Haemorrhage · Haematology in Pregnancy
- AREDS Classification of Age-related Macular Degeneration · Macular Degeneration
- Diabetic Macular Oedema (DMO) Classification · Diabetic Retinopathy
- Retinopathy of Prematurity — International Classification (ICROP3) · Paediatric Retina
- 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