Does DEXTROMETHORPHAN Cause Incorrect product administration duration? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Incorrect product administration duration have been filed in association with DEXTROMETHORPHAN (GUAIFENESIN DM). This represents 0.6% of all adverse event reports for DEXTROMETHORPHAN.
33
Reports of Incorrect product administration duration with DEXTROMETHORPHAN
0.6%
of all DEXTROMETHORPHAN reports
5
Deaths
6
Hospitalizations
How Dangerous Is Incorrect product administration duration From DEXTROMETHORPHAN?
Of the 33 reports, 5 (15.2%) resulted in death, 6 (18.2%) required hospitalization, and 5 (15.2%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN. However, 33 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which DEXTROMETHORPHAN Alternatives Have Lower Incorrect product administration duration 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