Registered Kenya · PPB

VABYSMO 6MG / 0.05ML SOLUTION FOR INJECTION

FARICIMAB

What it does

Faricimab is a medication used to treat certain eye conditions that can cause vision loss.

Commonly used for: diabetic macular edema (swelling in the eye due to diabetes), wet age-related macular degeneration (a type of vision loss in older adults)

Read more in plain English ↓

Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

Ask about this medicine

Answers come only from this medicine's registration record, BNF monograph and interaction data - not medical advice.

Hard to find? We help patients in Kenya source rare medicines. We don't sell or dispense medicines - licensed pharmacies do.

Source this medicine

Registration & product details

Registration no.
H2026/CTD11093/23041
Registration date
-
Expiry date
2031 June 07
Status
Registered
Active ingredient
FARICIMAB
Strength
-
Pack size
2ML TYPE I GLASS VIAL WITH A FLUORORESIN-LAMINATED BUTYL RUBBER STOPPER AND CRIMPED WITH AN ALUMINUM SEAL FITTED WITH A PLASTIC FLIP-OFF CAP CO-PACKAGED WITH A TRANSFER FILTER NEEDLE AND A LEAFLET IN A CARTON FOLDING BOX.
Therapeutic class
NEW/INNOVATOR
ATC class (WHO)
S01LA - Antineovascularisation agents
Drug group
SENSORY ORGANS
RxNorm RxCUI
2591519
Manufacturer / MAH
Roche
Applicant / LTR
F. HOFFMAN LA ROCHE
Country of origin
FOREIGN
Manufacturer location
Chaka Rd, Nairobi, Kenya

Source: Pharmacy and Poisons Board · fetched 2026-06-28 19:42:54 · updated 2026-10-30 02:05:44

Disclaimer: This information is sourced from Pharmacy and Poisons Board (Kenya). Always consult a qualified healthcare professional before using any medication.

About this medicine

Faricimab is a medication used to treat certain eye conditions that can cause vision loss.

What it treats

  • diabetic macular edema (swelling in the eye due to diabetes)
  • wet age-related macular degeneration (a type of vision loss in older adults)

How it works

Faricimab works by targeting specific proteins in the eye to reduce swelling and improve vision.

Who it's for

This medication is for adults with specific eye conditions that lead to vision problems.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: Faricimab

BNF-referenced

Faricimab is a bispecific immunoglobulin G1 antibody that acts as a dual inhibitor of angiopoietin-2 and vascular endothelial growth factor (VEGF), promoting vascular stability and reducing pathological angiogenesis. It is primarily used in the treatment of retinal disorders, particularly neovascular (wet) age-related macular degeneration (wAMD) and diabetic macular oedema (DMO).

Indications

  • Neovascular (wet) age-related macular degeneration
  • Diabetic macular oedema

Dosage

Children: There are no established pediatric dosing guidelines for Faricimab. For dosing in children, please refer to the BNF for Children.

Adults: The dosage for adults is determined by a specialist and varies based on the specific condition being treated. Please refer to the BNF for precise dosing guidelines.

Mechanism of action

Faricimab targets and inhibits both angiopoietin-2 (Ang-2) and vascular endothelial growth factor A (VEGF-A), which are key mediators in the regulation of vascular permeability and angiogenesis. By blocking these pathways, Faricimab restores vascular stability in the retina, thereby reducing edema and preventing vision loss associated with retinal diseases.

Pharmacodynamics

The pharmacodynamic effects of Faricimab include the reduction of retinal vascular leakage and the inhibition of neovascularization. The dual inhibition of Ang-2 and VEGF-A leads to improved retinal perfusion and stabilization of the retinal architecture, which is crucial in conditions characterized by abnormal blood vessel growth and leakage.

Pharmacokinetics

Faricimab is administered via intravitreal injection, allowing for direct delivery to the target site in the eye. Its pharmacokinetic profile shows a prolonged half-life due to its large molecular size and is characterized by a gradual clearance from the vitreous. Systemic absorption is minimal, leading to low systemic exposure. The drug is primarily eliminated through the reticuloendothelial system.

Contra-indications

  • Active intra-ocular inflammation
  • Ocular or periocular infection
  • Rhegmatogenous retinal detachment
  • Retinal tear
  • Stage 3 or 4 macular holes

Adverse effects

  • Endophthalmitis
  • Intra-ocular inflammation
  • Visual impairment
  • Retinal detachment

Precautions

  • Monitor intra-ocular pressure and perfusion of the optic nerve head following injection
  • Counsel patients to report symptoms suggestive of endophthalmitis or retinal detachment

Pregnancy

Avoid unless potential benefit outweighs risk; systemic exposure is very low.

Breast-feeding

Use with caution; limited excretion into milk expected and likely partially destroyed in the infant's gastrointestinal tract.

Storage

Store in a refrigerator (2–8°C); may be stored unopened at room temperature (20–25°C) for up to 24 hours before use; protect from light.

Formulations

  • Solution for injection (Brolucizumab 120 mg per 1 ml)
  • Solution for injection (Vabysmo)
BNF 85 (British National Formulary) p.1326 PubChem / pathway

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

This drug in other countries

The same active ingredient registered across other registries we cover - including different brands.