Indications & Dose:
Treatment of patients with Neovascular (Wet) Age-Related Macular Degeneration (AMD).
DOSAGE AND ADMINISTRATION
For ophthalmic intravitreal injection only.
The recommended dose is 2 mg (0.05 mL) administered by intravitreal injection every 4 weeks (monthly) for the first 3 months, followed by 2
mg (0.05 mL) via intravitreal injection once every 8 weeks (2 months). Although may be dosed as frequently as 2 mg every 4 weeks (monthly),
additional efficacy was not demonstrated when drug was dosed every 4 weeks compared to every 8 weeks.
Contraindications:
• Ocular or periocular infection
• Active intraocular inflammation
• Hypersensitivity
Side Effects:
Cautions:
Precautions:
Endophthalmitis and retinal detachments may occur following intravitreal injections. Patients should be instructed to report any symptoms
suggestive of endophthalmitis or retinal detachment without delay and should be managed appropriately.
• Increases in intraocular pressure have been seen within 60 minutes of an intravitreal injection.
Interaction:
Warnings:
Adverse Effects:
Lactations:
Special Precautions:
Counselling:
Side Effects Or Adverse Reactions:
The most common adverse reactions (=5%) reported in patients receiving were conjunctival hemorrhage, eye pain, cataract, vitreous
detachment, vitreous floaters, and increased intraocular pressure.
Patient And Carer Advice:
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