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Verteporfin

Photoenhancer — SENSORY ORGANS

Also known as: BPD-MA, trans-18-Ethenyl-4,4a-dihydro-3,4-bis(methoxycarbonyl)-4a,8,14,19-tetramethyl-23H,25H-benzo[b]porphine-9,13-dipropanoic acid monomethyl ester (1:1 mixture of two regioisomers), verteporphin, visudyne

EMA approvedFDA approvedATC S01LA01

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Verteporfin is a drug in the Photoenhancer class catalogued in DrugCentral. It was first approved by the FDA in 2000. Its mechanism of action is classified as Photoabsorption. Recorded indications include Choroidal retinal neovascularization, Exudative age-related macular degeneration, Ocular histoplasmosis syndrome and Pathologic Myopia.

  • Drug class: Photoenhancer.
  • Mechanism of action: Photoabsorption.
  • Indications: Choroidal retinal neovascularization, Exudative age-related macular degeneration, Ocular histoplasmosis syndrome and Pathologic Myopia.
  • ATC code: S01LA01 (Antineovascularisation agents).
  • Molecular formula: C82H84N8O16; molecular weight 1437.61 g/mol.

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (4)

  • Choroidal retinal neovascularization
  • Exudative age-related macular degeneration
  • Ocular histoplasmosis syndrome
  • Pathologic Myopia

Contraindications (3)

  • Breastfeeding (mother)
  • Disease of liver
  • Porphyria

Mechanism & targets

Mechanism of action (MoA)Photoabsorption
Established pharmacologic classPhotoenhancer

Regulatory approvals (2)

DateAgencyMarketed asApplicantOrphan
2000-07-27EMA——
2000-04-12FDA—VALEANT LUXEMBOURG

ATC classification

ATC codeTherapeutic hierarchy
S01LA01SENSORY ORGANS › OPHTHALMOLOGICALS › OCULAR VASCULAR DISORDER AGENTS › Antineovascularisation agents

Reported adverse-event signals

Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.

MedDRA termLLR
Visual acuity reduced1957.6
Retinal haemorrhage1141.6
Choroidal neovascularisation640.9
Polypoidal choroidal vasculopathy575.0
Retinal pigment epithelial tear467.7
Detachment of retinal pigment epithelium425.9
Disease progression396.5
Vitreous haemorrhage309.3
Retinal detachment295.3
Subretinal fluid234.2
Retinal degeneration218.0
Retinal oedema209.6

Chemical structure

Molecular formulaC82H84N8O16
Molecular weight1437.61 g/mol
CAS number129497-78-5
InChIKey—
PubChem CID5362420

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Verteporfin used for?

DrugCentral lists the following indications for Verteporfin: Choroidal retinal neovascularization, Exudative age-related macular degeneration, Ocular histoplasmosis syndrome and Pathologic Myopia.

How does Verteporfin work?

Verteporfin is classified as Photoabsorption.

When was Verteporfin first approved?

Verteporfin was first approved by the FDA in 2000.

What drug class does Verteporfin belong to?

Verteporfin is in the Photoenhancer class.

What is the chemical formula of Verteporfin?

Verteporfin has the molecular formula C82H84N8O16 and a molecular weight of 1437.61 g/mol.

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Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Quick facts

Status—
First approval2000-04-12
AgencyFDA
Targets0
Indications4
FormulaC82H84N8O16
DrugCentral ID2816
Interactive profile