Durysta: adverse event reports filed with FDA

468

reports as suspect product

0% of all reports · about 78 a year

51

reports, 12 months to June 2026

64 in the 12 months before

20.7%

marked serious by the reporter

27.8% across the class

0.4%

record death among outcomes, as reported

2 reports · not verified by FDA

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 Durysta reports recording the termmedian drug in prostaglandin analog

1. Intraocular pressure increasedraised pressure in the eye12.8%60
2. No adverse eventno adverse event was reported10%47
3. Product administered at inappropriate site9.4%44
4. Corneal oedema9.2%43
5. Iritis7.7%36
6. Complication of device insertion6.8%32
7. Device dislocationthe device moved out of position5.6%26
8. Eye paineye pain5.6%26
9. Needle issuea problem with the needle4.9%23
10. Eye inflammation4.3%20
11. Cystoid macular oedema4.1%19
12. Device malfunctionthe device did not work properly4.1%19
13. Vision blurredblurred vision4.1%19
14. Ocular hyperaemiaa red eye3.8%18
15. Drug ineffectivethe medicine did not work as expected3.4%16
16. Visual impairmentreduced vision3%14
17. Implantation complication2.8%13
18. Eye irritationeye irritation2.4%11
19. Photophobiasensitivity to light1.7%8
20. Visual acuity reducedreduced sharpness of vision1.7%8
21. Corneal endothelial cell loss1.5%7
22. Device deployment issuethe device did not deploy properly1.5%7
23. Device issuea problem with the device1.5%7
24. Endophthalmitisinfection inside the eye1.5%7
25. Product contamination physical1.5%7
26. Product quality issuea problem with the product itself1.5%7
27. Corneal decompensation1.3%6
28. Headachehead pain1.1%5
29. Uveitis1.1%5
30. Anterior chamber cell0.9%4

Top 30 of 70 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 median share across the 13 drugs in the prostaglandin analog class; 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 51,210 reports in the class. FDA has not verified any outcome and states that the reports "cannot be used to estimate the incidence of these events."

Patients and reporters

Age and sex as stated in the report; the reporter's qualification is the primary source recorded by FDA. 99.8% of reports give the United States as the country of the event or reporter.

Reason for use recorded

The indication field is filled in by the reporter and is often blank; shares are of all 468 reports.

Drugs most often listed in the same reports

Other products listed in reports where Durysta is a suspect product, whatever their own role. Co-listing means the two were recorded together; it says nothing about either product's part in the event. Only the 2,500 most-reported names are counted here.

In context

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."

Other drugs in the prostaglandin analog class

Ordered by report count for navigation only. 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." A brand and its generic are separate rows because reporters name them separately.

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 Durysta as a suspect or interacting product; reports listing it only as a concomitant medication (43) 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.