Does DIMETHICONE\LOPERAMIDE Cause Intentional product use issue? 194 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 194 reports of Intentional product use issue have been filed in association with DIMETHICONE\LOPERAMIDE. This represents 3.5% of all adverse event reports for DIMETHICONE\LOPERAMIDE.
194
Reports of Intentional product use issue with DIMETHICONE\LOPERAMIDE
3.5%
of all DIMETHICONE\LOPERAMIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intentional product use issue From DIMETHICONE\LOPERAMIDE?
Of the 194 reports.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIMETHICONE\LOPERAMIDE. However, 194 reports have been filed with the FAERS database.
What Other Side Effects Does DIMETHICONE\LOPERAMIDE Cause?
Drug ineffective (1,380)
Incorrect dose administered (892)
Dysphagia (549)
Product size issue (416)
Off label use (402)
Product packaging issue (348)
Wrong technique in product usage process (335)
Expired product administered (311)
Inappropriate schedule of drug administration (284)
Product use issue (259)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which DIMETHICONE\LOPERAMIDE Alternatives Have Lower Intentional product use issue Risk?
DIMETHICONE\LOPERAMIDE vs DIMETHINDENE
DIMETHICONE\LOPERAMIDE vs DIMETHYL
DIMETHICONE\LOPERAMIDE vs DIMETHYL SULFONE
DIMETHICONE\LOPERAMIDE vs DINOPROSTONE
DIMETHICONE\LOPERAMIDE vs DINUTUXIMAB