Visudyne

Visudyne

verteporfin

Manufacturer:

Zuellig Pharma

Distributor:

Zuellig Pharma
Concise Prescribing Info
Contents
Verteporfin
Indications/Uses
Predominantly classic or occult subfoveal choroidal neovascularization due to age-related macular degeneration or w/ subfoveal choroidal neovascularization caused by other macular disease.
Dosage/Direction for Use
1st step: 6 mg/m2 as 10-min IV infusion. 2nd step: Light activation at 15 min after start of infusion. Recurrent CNV leakage Re-evaluate every 3 mth.
Contraindications
Special Precautions
Discontinue use if anaphylactic or other serious allergic reaction occurs. Photosensitivity up to 48 hr after infusion. Severe decreased vision (equiv ≥4 lines) w/in 1 wk after treatment. Avoid extravasation. May affect ability to drive or use machines. Moderate to severe hepatic impairment or biliary obstruction. Renal impairment. Pregnancy & lactation. Not to be used in childn.
Adverse Reactions
Retinal detachment, haemorrhage, ischaemia & oedema, vitreous haemorrhage, visual impairment & field defect, reduced visual acuity, nausea, asthenia, inj site oedema, inflammation, extravasation, pain, hypersensitivity & haemorrhage, pyrexia, back & chest pain, hypoaesthesia, photosensitivity reaction, HTN, syncope, malaise, headache, dizziness, dyspnoea, rash, urticaria, pruritus.
Drug Interactions
Increased potential photosensitivity reactions w/ photosensitising agents. Enchanced tissue-uptake w/ Ca-channel blockers, polymyxin B, radiation therapy. Decreased activity w/ antioxidants (eg, β-carotene) or free radical scavengers (eg, dimethylsulfoxide, formate, mannitol, alcohol). Antagonized action w/ vasodilators & drugs diminishing clotting & platelet aggregation (eg, thromboxane A2 inhibitors).
MIMS Class
Other Eye Preparations
ATC Classification
S01LA01 - verteporfin ; Belongs to the class antineovasculatisation agents. Used in the management of neovascular macular degeneration.
Presentation/Packing
Form
Visudyne infusion 15 mg
Packing/Price
1's
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