Does MENTHOL\ZINC Cause Incorrect product administration duration? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Incorrect product administration duration have been filed in association with MENTHOL\ZINC. This represents 1.4% of all adverse event reports for MENTHOL\ZINC.
6
Reports of Incorrect product administration duration with MENTHOL\ZINC
1.4%
of all MENTHOL\ZINC reports
6
Deaths
6
Hospitalizations
How Dangerous Is Incorrect product administration duration From MENTHOL\ZINC?
Of the 6 reports, 6 (100.0%) resulted in death, 6 (100.0%) required hospitalization, and 6 (100.0%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MENTHOL\ZINC. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does MENTHOL\ZINC Cause?
Pain (180)
Mesothelioma (123)
Anxiety (91)
Loss of personal independence in daily activities (81)
Occupational exposure to product (81)
Drug ineffective (68)
Lung neoplasm malignant (68)
Off label use (67)
Exposure to chemical pollution (56)
Injury (56)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which MENTHOL\ZINC Alternatives Have Lower Incorrect product administration duration Risk?
MENTHOL\ZINC vs MEPERIDINE
MENTHOL\ZINC vs MEPIVACAINE
MENTHOL\ZINC vs MEPIVACAINE\MEPIVACAINE
MENTHOL\ZINC vs MEPOLIZUMAB
MENTHOL\ZINC vs MEPROBAMATE