Yutiq: adverse event reports filed with FDA

736

reports as suspect product

0% of all reports · about 103 a year

80

reports, 12 months to June 2026

154 in the 12 months before

6%

marked serious by the reporter

77.7% across the class

0%

record death among outcomes, as reported

0 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

Reactions recorded in the reports

share of Yutiq reports recording the termmedian drug in corticosteroid

1. Off label useused for a purpose or in a way not on the label55.7%410
2. Product dose omission issuea dose was missed17.3%127
3. No adverse eventno adverse event was reported16.4%121
4. Needle issuea problem with the needle7.9%58
5. Circumstance or information capable of leading to medication errora situation that could lead to a medication error7.3%54
6. Device dislocationthe device moved out of position7.3%54
7. Drug delivery system issue5.8%43
8. Product quality issuea problem with the product itself5.8%43
9. Device failurethe device failed5.4%40
10. Medical device removalthe device was removed3.8%28
11. Drug delivery system malfunction3.5%26
12. Complication of device insertion3.4%25
13. Implantation complication3%22
14. Device malfunctionthe device did not work properly1.9%14
15. Drug ineffectivethe medicine did not work as expected1.9%14
16. Product administration errora mistake in giving the product1.9%14
17. Corneal oedema1.5%11
18. Drug dose omission by device1.4%10
19. Device dispensing error1.2%9
20. Device difficult to usethe device was hard to use1%7
21. Device issuea problem with the device1%7
22. Intraocular pressure increasedraised pressure in the eye0.8%6
23. Eye inflammation0.7%5
24. Syringe issue0.7%5
25. Visual impairmentreduced vision0.7%5
26. Macular oedema0.5%4
27. Patient uncooperative0.5%4
28. Product dose omissiona dose was missed0.5%4
29. Discomfortdiscomfort0.4%3
30. Condition aggravatedthe condition being treated got worse0.3%2

Top 30 of 55 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 74 drugs in the corticosteroid 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 808,789 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. 99.9% 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 736 reports.

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 corticosteroid 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 Yutiq as a suspect or interacting product; reports listing it only as a concomitant medication (4) 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.