Does MICONAZOLE Cause Recalled product administered? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Recalled product administered have been filed in association with MICONAZOLE (Zeasorb Athletes Foot). This represents 0.2% of all adverse event reports for MICONAZOLE.
13
Reports of Recalled product administered with MICONAZOLE
0.2%
of all MICONAZOLE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Recalled product administered From MICONAZOLE?
Of the 13 reports, 2 (15.4%) required hospitalization, and 1 (7.7%) were considered life-threatening.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MICONAZOLE. However, 13 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which MICONAZOLE Alternatives Have Lower Recalled product administered Risk?
MICONAZOLE vs MIDAZOLAM
MICONAZOLE vs MIDAZOLAM\MIDAZOLAM
MICONAZOLE vs MIDODRINE
MICONAZOLE vs MIDOMAFETAMINE
MICONAZOLE vs MIDOSTAURIN