Does DEXTROMETHORPHAN Cause Wrong technique in product usage process? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Wrong technique in product usage process have been filed in association with DEXTROMETHORPHAN (GUAIFENESIN DM). This represents 0.6% of all adverse event reports for DEXTROMETHORPHAN.
31
Reports of Wrong technique in product usage process with DEXTROMETHORPHAN
0.6%
of all DEXTROMETHORPHAN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DEXTROMETHORPHAN?
Of the 31 reports, 1 (3.2%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN. However, 31 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DEXTROMETHORPHAN Alternatives Have Lower Wrong technique in product usage process 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