Miconazole: adverse event reports filed with FDA

650

reports as suspect product

0% of all reports · about 29 a year

30

reports, 12 months to June 2026

12 in the 12 months before

72.3%

marked serious by the reporter

79% across the class

6%

record death among outcomes, as reported

39 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 Miconazole reports recording the termmedian drug in azole antifungal

1. Drug interactionan interaction between medicines30%195
2. International normalised ratio increasedblood clotting slower than intended (raised INR)17.8%116
3. Drug ineffectivethe medicine did not work as expected12.8%83
4. Haematuriablood in the urine4.8%31
5. Anaphylactoid reaction2.6%17
6. Pruritusitching2.5%16
7. Burning sensationa burning feeling2.3%15
8. Vulvovaginal burning sensation2.3%15
9. Application site pain2.2%14
10. Drug hypersensitivityan allergic-type reaction to a medicine2%13
11. Haemorrhage subcutaneous1.8%12
12. Nauseafeeling sick1.8%12
13. Off label useused for a purpose or in a way not on the label1.8%12
14. Medication errora mistake in prescribing, dispensing or taking a medicine1.5%10
15. Muscular weaknessmuscle weakness1.5%10
16. Pyrexiafever1.5%10
17. Somnolencedrowsiness1.5%10
18. Astheniaweakness or lack of energy1.4%9
19. Cerebral haemorrhage1.4%9
20. Contusiona bruise1.4%9
21. Eosinophilia1.4%9
22. Pericarditisinflammation of the sac around the heart1.4%9
23. Platelet count decreasedlow platelet count1.4%9
24. Urticariahives1.4%9
25. Confusional stateconfusion1.2%8
26. Infective keratitis1.2%8
27. Oedema genital1.2%8
28. Rash erythematousa red rash1.2%8
29. Rash pustular1.2%8
30. Urinary tract infectionbladder or urinary infection1.2%8

Top 30 of 267 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 16 drugs in the azole antifungal 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 69,035 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. 36.8% 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 650 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 azole antifungal 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 Miconazole as a suspect or interacting product; reports listing it only as a concomitant medication (1,655) 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.