Does LOPERAMIDE Cause Incorrect product administration duration? 543 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 543 reports of Incorrect product administration duration have been filed in association with LOPERAMIDE (Anti-diarrheal). This represents 3.0% of all adverse event reports for LOPERAMIDE.
543
Reports of Incorrect product administration duration with LOPERAMIDE
3.0%
of all LOPERAMIDE reports
1
Deaths
3
Hospitalizations
How Dangerous Is Incorrect product administration duration From LOPERAMIDE?
Of the 543 reports, 1 (0.2%) resulted in death, 3 (0.6%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LOPERAMIDE. However, 543 reports have been filed with the FAERS database.
What Other Side Effects Does LOPERAMIDE Cause?
Drug ineffective (3,207)
Diarrhoea (1,909)
Constipation (1,614)
Off label use (1,378)
Incorrect dose administered (1,178)
Drug abuse (1,088)
Nausea (997)
Intentional product use issue (871)
Overdose (857)
Toxicity to various agents (753)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
ALENDRONATE (287)
Which LOPERAMIDE Alternatives Have Lower Incorrect product administration duration Risk?
LOPERAMIDE vs LOPINAVIR
LOPERAMIDE vs LOPINAVIR\RITONAVIR
LOPERAMIDE vs LOPRAZOLAM
LOPERAMIDE vs LORATADINE
LOPERAMIDE vs LORATADINE\PSEUDOEPHEDRINE