Brand name · Verteporfin for injection
Visudyne: adverse event reports filed with FDA
1,348 reports list it as a suspect or interacting product, 2004–2026.
- 1,348
- reports as suspect product
- 0% of all reports · about 60 a year
- 6
- reports, 12 months to June 2026
- 2 in the 12 months before
- 88.2%
- marked serious by the reporter
- 57.4% across all reports
- 3.7%
- record death among outcomes, as reported
- 50 reports · not verified by FDA
1,348 adverse event reports received by FDA list the brand name Visudyne (verteporfin for injection) as a suspect or interacting product, from February 2004 to June 2026. A further 119 reports list it only as a concomitant medication, and those are not counted in the figures on this page.
In the 12 months to June 2026, 6 reports listed it, up 200% from 2 in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Over its reporting history that is about 60 reports a year and 0% of the 20,646,523 reports in the database. How many people take it is not in the data, so a count is not a rate of occurrence.
The MedDRA terms listed most often are visual acuity reduced (26.6%), retinal haemorrhage (13.3%) and disease progression (11.9%). A report can list several reactions, so shares add to more than 100%; 235 different terms appear across these reports. Visual acuity reduced is recorded in 26.6% of these reports, against 0.2% of all reports in the database.
88.2% of the reports are marked serious by the reporter; 3.7% record death among the outcomes and 12% record hospitalisation, as reported. 69.7% of the reports came from physicians, and the largest patient age group is 75 and over (34.1%). FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event."
Reports by month, five years
Reports by the month FDA received them. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases.
By year received
2026 covers reports received through June 2026 only.
Reactions recorded in the reports
share of Visudyne reports recording the termall reports in the database
- Visual acuity reducedreduced sharpness of vision26.6%359
- Retinal haemorrhage13.3%179
- Disease progressionthe disease advanced11.9%160
- Off label useused for a purpose or in a way not on the label9.6%129
- Polypoidal choroidal vasculopathy9.6%129
- Choroidal neovascularisation7%94
- Age-related macular degeneration6.2%84
- Retinal pigment epithelial tear4.3%58
- Retinal detachmentthe retina separated from the back of the eye4.2%57
- Macular degenerationa disease of the central retina4%54
- Detachment of retinal pigment epithelium3.9%52
- Condition aggravatedthe condition being treated got worse3.6%48
- Product use in unapproved indicationused for a purpose not on the label3.3%44
- Vitreous haemorrhage3.3%44
- Back painback pain2.7%37
- Macular oedema2.2%29
- Retinal oedema2%27
- Cystoid macular oedema1.8%24
- Metamorphopsia1.8%24
- Drug ineffectivethe medicine did not work as expected1.6%21
- Macular hole1.6%21
- Subretinal fluid1.6%21
- Blindnessloss of sight1.5%20
- Chorioretinal disorder1.5%20
- Cataractclouding of the eye lens1.4%19
- Retinal degeneration1.4%19
- Retinal disorder1.4%19
- Subretinal fibrosis1.4%19
- Eye haemorrhage1.3%17
- Infusion related reactiona reaction during or soon after an infusion1.3%17
Top 30 of 235 MedDRA preferred terms recorded across these reports, with a plain-language gloss where one is available. One report can record several terms. The hollow bar is the share of all reports in the database; it describes the reports, not the patients. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."
Outcomes recorded
Outcome flags as the reporter set them; a report can carry several, and "other serious" is FDA's own category for serious reports outside the named outcomes. Grey bar: all 20,646,523 reports. FDA has not verified any outcome and states that the reports "cannot be used to estimate the incidence of these events."
Patients and reporters
Patient age
Patient sex
Who reported
Age and sex as stated in the report; the reporter's qualification is the primary source recorded by FDA. 26.3% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Macular degeneration | 319 | 23.7% |
| Age-related macular degeneration | 203 | 15.1% |
| Polypoidal choroidal vasculopathy | 181 | 13.4% |
| Choroidal neovascularisation | 134 | 9.9% |
| Chorioretinopathy | 89 | 6.6% |
| Product use in unapproved indication | 15 | 1.1% |
The indication field is filled in by the reporter and is often blank; shares are of all 1,348 reports.
In context
| Measure | Visudyne | All reports |
|---|---|---|
| Reports as suspect product | 1,348 | 20,646,523 |
| Share of that pool | — | 0% |
| Reports, latest 12 months | 6 | 1,332,454 |
| Marked serious | 88.2% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 37 | 91 |
| Hospitalisation recorded, per 1,000 reports | 120 | 213 |
| Consumer-filed share | 8.2% | 45.8% |
| Top term, share of reports | Visual acuity reduced 26.6% | 0.2% |
Shares are of reports, not of patients treated. The number of people taking a product is not in the data, so none of these figures is a rate, and differences between columns reflect who takes a product, who reports and how long it has been sold. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."
Questions about Visudyne reports
How many adverse event reports has FDA received for Visudyne?
1,348 reports list Visudyne as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 6 of them arrived in the latest 12 months. Another 119 list it only as a concomitant medication.
What reactions are recorded in Visudyne reports?
visual acuity reduced (26.6%), retinal haemorrhage (13.3%), disease progression (11.9%), off label use (9.6%) and polypoidal choroidal vasculopathy (9.6%). These are MedDRA preferred terms coded from what the reporter described; a report can list several, and a term's presence is not a finding that Visudyne was responsible.
How serious are the reports?
88.2% are marked serious by the reporter. Among the outcomes recorded, 3.7% of reports include death and 12% include hospitalisation. FDA has not verified these outcomes and states that the reports "cannot be used to estimate the incidence" of the events.
Who files these reports?
physician (69.7%), other health professional (18%) and consumer or non-health professional (8.2%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Visudyne rising?
6 reports in the 12 months to June 2026, up 200% from 2 in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Counts also move with how many people take a product, its time on the market and publicity.
Do these reports show that Visudyne was responsible for these reactions?
No. FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event." The reaction may relate to the condition being treated, to other medicines, or to something else.
Is this a list of the side effects of Visudyne?
No. It is a count of what was reported to FDA. The adverse reactions observed in clinical studies are printed on the FDA-approved label, which a pharmacist or clinician can go through with you.
How do I report an adverse event?
Consumers and health professionals can report to FDA through MedWatch (Form FDA 3500 online, or 1-800-FDA-1088), or to the manufacturer, which must pass reports on. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Drug Adverse Event (FAERS) bulk export released 28 Sep 2026, which holds reports FDA received through 30 Jun 2026. Drug names are as reported, resolved to the brand or generic name on the FDA label where openFDA's harmonisation matched them; classes are the pharmacologic class (EPC) from the label and the National Drug Code Directory of 17 Sep 2026. A report counts here when it lists Visudyne as a suspect or interacting product; reports listing it only as a concomitant medication (119) are excluded. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.