DOSING CALCULATOR
Patient’s body surface area (BSA)
Input your patient's information below to calculate
- Patient’s body weight
- Patient’s height
Patient is 00 lbs, 0 ft 0 inches
| Body surface area(BSA) | = | 0.00 | m2 | ||||||||||||
| Total drug dose(6 mg/m2 x BSA) | = | 00.0 | mg | ||||||||||||
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Input your patient's information below to calculate
| Body surface area(BSA) | = | 0.00 | m2 | ||||||||||||
| Total drug dose(6 mg/m2 x BSA) | = | 00.0 | mg | ||||||||||||
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Please be sure to have a strong, viable, open vein before reconstituting the VISUDYNE®.

* Reconstituted VISUDYNE® must be protected from light and used within 4 hours. It is recommended that reconstituted VISUDYNE® be inspected visually for particulate matter and discoloration prior to administration. Reconstituted VISUDYNE® is an opaque dark green solution.
VISUDYNE® (verteporfin for injection) therapy is a photoenhancer indicated for the treatment of patients with predominantly classic subfoveal choroidal neovascularization (CNV) due to age-related macular degeneration, pathologic myopia or presumed ocular histoplasmosis. There is insufficient evidence to indicate VISUDYNE for the treatment of predominantly occult subfoveal CNV.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.
Click here for full Prescribing Information for VISUDYNE®.
Indication and Important Safety Information
References: 1. VISUDYNE [package insert]. Bridgewater, NJ: Bausch & Lomb Incorporated.