Does MICONAZOLE Cause Product use issue? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Product use issue have been filed in association with MICONAZOLE (Zeasorb Athletes Foot). This represents 0.6% of all adverse event reports for MICONAZOLE.
35
Reports of Product use issue with MICONAZOLE
0.6%
of all MICONAZOLE reports
1
Deaths
1
Hospitalizations
How Dangerous Is Product use issue From MICONAZOLE?
Of the 35 reports, 1 (2.9%) resulted in death, 1 (2.9%) required hospitalization, and 2 (5.7%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MICONAZOLE. However, 35 reports have been filed with the FAERS database.
What Other Side Effects Does MICONAZOLE Cause?
Vulvovaginal burning sensation (1,870)
Drug ineffective (1,170)
Vulvovaginal pain (1,036)
Vulvovaginal pruritus (651)
Vaginal haemorrhage (543)
Condition aggravated (524)
Vulvovaginal discomfort (487)
Vulvovaginal swelling (419)
Burning sensation (177)
Vaginal discharge (172)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which MICONAZOLE Alternatives Have Lower Product use issue Risk?
MICONAZOLE vs MIDAZOLAM
MICONAZOLE vs MIDAZOLAM\MIDAZOLAM
MICONAZOLE vs MIDODRINE
MICONAZOLE vs MIDOMAFETAMINE
MICONAZOLE vs MIDOSTAURIN