Does DEXTROMETHORPHAN Cause Product complaint? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Product complaint have been filed in association with DEXTROMETHORPHAN (GUAIFENESIN DM). This represents 0.4% of all adverse event reports for DEXTROMETHORPHAN.
22
Reports of Product complaint with DEXTROMETHORPHAN
0.4%
of all DEXTROMETHORPHAN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product complaint From DEXTROMETHORPHAN?
Of the 22 reports, 1 (4.5%) required hospitalization.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN. However, 22 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 complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
Which DEXTROMETHORPHAN Alternatives Have Lower Product complaint 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