Does DIMETHICONE\LOPERAMIDE Cause Product packaging quantity issue? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product packaging quantity issue have been filed in association with DIMETHICONE\LOPERAMIDE. This represents 0.1% of all adverse event reports for DIMETHICONE\LOPERAMIDE.
7
Reports of Product packaging quantity issue with DIMETHICONE\LOPERAMIDE
0.1%
of all DIMETHICONE\LOPERAMIDE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product packaging quantity issue From DIMETHICONE\LOPERAMIDE?
Of the 7 reports.
Is Product packaging quantity issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIMETHICONE\LOPERAMIDE. However, 7 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 Product packaging quantity issue?
LEUPROLIDE (523)
ALBUTEROL (431)
BUDESONIDE\FORMOTEROL (301)
FENTANYL (286)
BUPRENORPHINE (225)
CYCLOSPORINE (206)
ESTRADIOL (201)
BIMATOPROST (177)
RIVAROXABAN (174)
EXENATIDE (154)
Which DIMETHICONE\LOPERAMIDE Alternatives Have Lower Product packaging quantity issue Risk?
DIMETHICONE\LOPERAMIDE vs DIMETHINDENE
DIMETHICONE\LOPERAMIDE vs DIMETHYL
DIMETHICONE\LOPERAMIDE vs DIMETHYL SULFONE
DIMETHICONE\LOPERAMIDE vs DINOPROSTONE
DIMETHICONE\LOPERAMIDE vs DINUTUXIMAB