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verteporfin

Photosensitiser for photodynamic therapy (benzoporphyrin derivative) · Anti-angiogenic

START
6 mg/m² IV over 10 min, then 689-nm laser at 15 min
TYPICAL MAX
6 mg/m² per session
STOP IF
Severe hypersensitivity or significant subretinal haemorrhage
WATCH
Strict 48-h sun/bright-light avoidance after infusion
CDSCO approvedATC S01LA01
Renal dose adjustmenteGFR mL/min/1.73m²
FULLNo dose adjustment at any eGFR90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
6minONSET15minPEAK5.5h2dDURATION
ONSET
6min · infusion start
PEAK
15min · laser activation
5.5h ·
DURATION
2d · photosens cover
EXCRETION
Faecal predominant; minimal renal
route + CYP
INTERACTIONS
2 major
SEVERE in our sources
PREGNANCY
Use only if benefit outweighs risk.
FDA category + note
Top interactionssee all 3
  • Aminolevulinic AcidSevereDatabaseDDInter
  • SunlightSevereDatabaseKimi deep-research + Cla

Mechanism

Lipophilic photosensitiser taken up via LDL receptors by abnormal endothelium of neovascular lesions; activated by 689-nm light to generate reactive oxygen species, occluding pathologic vessels in choroidal neovascularisation.

Indications

Predominantly classic choroidal neovascularisation in age-related macular degenerationPathologic myopia / ocular histoplasmosis-associated CNV (selected)

Dosing

Adult
6 mg/m² IV over 10 min, then light activation (689 nm laser) at 15 min after infusion start; repeat as indicated up to every 3 months.
Pediatric
Not established.
Renal adjustment
No specific adjustment.
Hepatic adjustment
Avoid in severe hepatic impairment.
Geriatric
No specific adjustment.
Max dose
6 mg/m² per session

Pharmacokinetics

Onset
Photoactivation immediate with laser
Peak effect
End of infusion
Duration
Vascular closure within ~30 min of light
Half-life
~5–6 h
Bioavailability
IV 100%
Protein binding
~90% (lipoproteins)
Metabolism
Hepatic / plasma esterase to inactive diacid
Excretion
Faecal (predominant); minimal renal

Contraindications

  • Porphyria
  • Severe hepatic impairment
  • Hypersensitivity

Side effects

Common
Injection-site reactions/back pain (infusion)Visual disturbanceHeadachePhotosensitivity
Serious
  • Severe photosensitivity reactions / sunburn (48 h)
  • Anaphylaxis / vasovagal reactions
  • Severe vision loss (rare; subretinal haemorrhage)

Pregnancy & lactation

Pregnancy

Use only if benefit outweighs risk.

Lactation

Interrupt breastfeeding for 48 h post-infusion.

Drug interactions

Aminolevulinic Acid
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Sunlight
Severe
Database

Photosensitisation

Strict 48-h avoidance; cover skin/eyes

Source: Kimi deep-research + Cla

Other Photosensitising Drugs
Moderate
Database

Additive photosensitivity

Caution and counselling

Source: Kimi deep-research + Cla

9 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.

Related guidelines

Ask House about verteporfin

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: Goodman & Gilman 14e·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20