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
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 class | Photoenhancer |
Regulatory approvals (2)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2000-07-27 | EMA | — | — | |
| 2000-04-12 | FDA | — | VALEANT LUXEMBOURG |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
S01LA01 | SENSORY 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 term | LLR |
|---|---|
| Visual acuity reduced | 1957.6 |
| Retinal haemorrhage | 1141.6 |
| Choroidal neovascularisation | 640.9 |
| Polypoidal choroidal vasculopathy | 575.0 |
| Retinal pigment epithelial tear | 467.7 |
| Detachment of retinal pigment epithelium | 425.9 |
| Disease progression | 396.5 |
| Vitreous haemorrhage | 309.3 |
| Retinal detachment | 295.3 |
| Subretinal fluid | 234.2 |
| Retinal degeneration | 218.0 |
| Retinal oedema | 209.6 |
Chemical structure
| Molecular formula | C82H84N8O16 |
|---|---|
| Molecular weight | 1437.61 g/mol |
| CAS number | 129497-78-5 |
| InChIKey | — |
| PubChem CID | 5362420 |
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.
Browse: all drugs starting with V · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 2816 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL5314346 — compound record and bioactivity
- PubChem CID 5362420 — chemical identifiers
- DrugBank DB00460 — drug record
- FDA UNII 0X9PA28K43 — substance identity
- DailyMed: FDA labels for Verteporfin — current prescribing information (label search)
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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.