Does DEXTROMETHORPHAN Cause Off label use? 83 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 83 reports of Off label use have been filed in association with DEXTROMETHORPHAN (GUAIFENESIN DM). This represents 1.6% of all adverse event reports for DEXTROMETHORPHAN.
83
Reports of Off label use with DEXTROMETHORPHAN
1.6%
of all DEXTROMETHORPHAN reports
36
Deaths
55
Hospitalizations
How Dangerous Is Off label use From DEXTROMETHORPHAN?
Of the 83 reports, 36 (43.4%) resulted in death, 55 (66.3%) required hospitalization, and 31 (37.3%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN. However, 83 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 Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which DEXTROMETHORPHAN Alternatives Have Lower Off label use 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