osudhkosh

Generic

Brolucizumab

1 brands available in the market

At a glance

Brolucizumab is a human VEGF inhibitor used for the treatment of Neovascular (Wet) Age-Related Macular Degeneration (AMD) and Diabetic Macular Edema (DME).

Description

Brolucizumab is a human VEGF inhibitor that binds to the three major isoforms of VEGF-A (VEGF 110, VEGF 121, and VEGF 165), thereby preventing interaction with receptors VEGFR-1 and VEGFR-2. By inhibiting VEGF-A, brolucizumab suppresses endothelial cell proliferation, neovascularization, and vascular permeability.

Indications
  • Neovascular (Wet) Age-Related Macular Degeneration (AMD)
  • Diabetic Macular Edema (DME)
Therapeutic class

Ophthalmic Preparations

Pharmacological class

VEGF Inhibitor

Pharmacology

Brolucizumab is a human VEGF inhibitor that binds to the three major isoforms of VEGF-A, thereby preventing interaction with receptors VEGFR-1 and VEGFR-2. By inhibiting VEGF-A, brolucizumab suppresses endothelial cell proliferation, neovascularization, and vascular permeability.

Mechanism of action

Brolucizumab binds to VEGF-A, inhibiting vascular endothelial growth factor, which reduces abnormal blood vessel growth and fluid leakage, improving vision.

Dosage

Neovascular AMD: 6 mg (0.05 mL) monthly for first 3 doses, then 6 mg every 8-12 weeks.
Diabetic Macular Edema (DME): 6 mg every 6 weeks for first 5 doses, then 6 mg every 8-12 weeks.

Administration

This medicine is given as an intravitreal injection by an ophthalmologist.

Missed dose

Brolucizumab is an injection medicine given by healthcare professionals. You cannot miss a dose yourself.

Side effects

Common: Vision blurred, cataract, conjunctival hemorrhage, eye pain, vitreous floaters.

Precautions & warnings

Endophthalmitis and retinal detachment may occur; report symptoms immediately. Retinal vasculitis/occlusion has been reported. IOP increase may occur within 30 minutes of injection. Potential risk of ATE.

Contraindications

Ocular or periocular infections; active intraocular inflammation; hypersensitivity to any component.

Drug interactions

No adequate information on drug interactions is available.

Food interactions

Can be used with or without food.

Use in pregnancy

No adequate and well-controlled studies in pregnant women. Animal studies showed fetal loss and abnormality at 10-fold MRHD.

Pregnancy Category: N/A — always consult a doctor before taking during pregnancy.

Use in lactation

No information on presence in human milk. Breastfeeding is not recommended during treatment and for at least one month after the last dose.

Pediatric use

Safety and efficacy in pediatric patients have not been established.

Geriatric use

No specific dosage adjustment is necessary for elderly patients.

Renal / hepatic impairment

No special precautions are necessary for patients with kidney or liver problems.

Overdose effects

No adequate information on overdose is available.

Storage conditions

Refrigerate at 2-8°C (do not freeze). Store in outer carton to protect from light. May be kept at 20-25°C for up to 24 hours prior to use.

Chemical structure

Brolucizumab

Common questions

What is Brolucizumab used for?
It is used for Neovascular (Wet) AMD and Diabetic Macular Edema (DME).
What is the dosage?
AMD: 6 mg monthly for 3 doses, then every 8-12 weeks; DME: 6 mg every 6 weeks for 5 doses, then every 8-12 weeks.
What are the common side effects?
Vision blurred, cataract, eye pain, conjunctival hemorrhage, vitreous floaters.
Who should not use it?
Patients with ocular infections, active intraocular inflammation, or hypersensitivity.
Can it be used during pregnancy?
Consult your doctor.
⚠️ This information is for educational purposes only — not a substitute for medical advice. Consult a registered physician before taking any medicine.