Verteporfin (Specialist drug)
Brand names: Visudyne
Verteporfin is a specialist photosensitising agent used in photodynamic therapy, classically for choroidal neovascularisation such as in age-related macular degeneration.
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
After intravenous administration it accumulates in abnormal neovascular tissue; subsequent activation by a non-thermal laser of specific wavelength generates reactive oxygen species that occlude the targeted vessels.
Prescribing in practice
- Patients become transiently photosensitive and must avoid exposure of skin and eyes to bright light and direct sunlight for the period stated in the SPC to prevent severe phototoxic reactions.
- It is administered by intravenous infusion followed by timed laser activation under specialist ophthalmology supervision.
- Extravasation should be avoided as it can cause local tissue damage, and infusion site reactions can occur.
Monitoring
Monitor the infusion site for extravasation, assess visual outcomes at follow-up, and reinforce strict light-avoidance precautions during the photosensitive period.
Counselling the patient
- Avoid direct sunlight and bright indoor lights for the period your team specifies, as your skin and eyes will be very sensitive.
- If you must go outside, cover exposed skin and wear dark sunglasses; ordinary sunscreen does not protect against this reaction.
- Report any infusion-site pain or skin reactions to your team.
Evidence & guidelines
Photodynamic therapy with verteporfin for neovascular AMD was established by the TAP study and remains a recognised specialist option in selected cases.
Reference: SmPC; 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).
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