Upneeq: adverse event reports filed with FDA

1,701

reports as suspect product

0% of all reports · about 296 a year

270

reports, 12 months to June 2026

281 in the 12 months before

5.1%

marked serious by the reporter

41.3% across the class

0.1%

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 Upneeq reports recording the termmedian drug in vasoconstrictor

1. Drug ineffectivethe medicine did not work as expected18.6%316
2. Vision blurredblurred vision14.8%251
3. Eye irritationeye irritation12.5%213
4. Ocular hyperaemiaa red eye12.3%209
5. Off label useused for a purpose or in a way not on the label9.6%164
6. Headachehead pain8.8%149
7. Dry eyedry eye8.1%138
8. Eye paineye pain8.1%138
9. Mydriasis7%119
10. Eye pruritus5.2%88
11. Lacrimation increasedwatery eyes4.4%75
12. Swelling of eyelid4.4%74
13. Eye swellinga swollen eye3.5%59
14. Dizzinesslight-headedness or unsteadiness2.8%47
15. Blood pressure increaseda raised blood pressure reading2.4%40
16. Therapeutic product effect decreased2.1%35
17. Therapeutic product effect incomplete1.8%31
18. Eyelid disorder1.8%30
19. Erythema of eyelid1.6%28
20. Foreign body sensation in eyes1.6%28
21. Photophobiasensitivity to light1.6%28
22. Ocular discomfort1.6%27
23. Asthenopia1.5%26
24. Drug effect less than expected1.5%26
25. Eye discharge1.5%26
26. Prescription drug used without a prescription1.5%25
27. Multiple use of single-use product1.4%24
28. Migrainemigraine1.2%21
29. Visual impairmentreduced vision1.2%20
30. Product administration errora mistake in giving the product1.1%19

Top 30 of 140 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 4 drugs in the vasoconstrictor 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 4,013 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. 100% 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 1,701 reports.

Drugs most often listed in the same reports

Other products listed in reports where Upneeq 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 vasoconstrictor 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 Upneeq as a suspect or interacting product; reports listing it only as a concomitant medication (39) 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.