Does DEXTROMETHORPHAN Cause Product use issue? 57 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Product use issue have been filed in association with DEXTROMETHORPHAN (GUAIFENESIN DM). This represents 1.1% of all adverse event reports for DEXTROMETHORPHAN.
57
Reports of Product use issue with DEXTROMETHORPHAN
1.1%
of all DEXTROMETHORPHAN reports
25
Deaths
25
Hospitalizations
How Dangerous Is Product use issue From DEXTROMETHORPHAN?
Of the 57 reports, 25 (43.9%) resulted in death, 25 (43.9%) required hospitalization, and 20 (35.1%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN. However, 57 reports have been filed with the FAERS database.
What Other Side Effects Does DEXTROMETHORPHAN Cause?
Drug ineffective (1,204)
Drug abuse (625)
Toxicity to various agents (618)
Overdose (504)
Accidental overdose (356)
Dizziness (339)
Completed suicide (289)
Diarrhoea (270)
No adverse event (240)
Death (213)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which DEXTROMETHORPHAN Alternatives Have Lower Product use issue Risk?
DEXTROMETHORPHAN vs DEXTROMETHORPHAN HYDROBROMIDE
DEXTROMETHORPHAN vs DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN
DEXTROMETHORPHAN vs DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN\PHENYLEPHRINE
DEXTROMETHORPHAN vs DEXTROMETHORPHAN HYDROBROMIDE\QUINIDINE
DEXTROMETHORPHAN vs DEXTROMETHORPHAN\GUAIFENESIN