Does DEXTROMETHORPHAN\GUAIFENESIN Cause Product use complaint? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Product use complaint have been filed in association with DEXTROMETHORPHAN\GUAIFENESIN. This represents 4.2% of all adverse event reports for DEXTROMETHORPHAN\GUAIFENESIN.
18
Reports of Product use complaint with DEXTROMETHORPHAN\GUAIFENESIN
4.2%
of all DEXTROMETHORPHAN\GUAIFENESIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product use complaint From DEXTROMETHORPHAN\GUAIFENESIN?
Of the 18 reports.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN\GUAIFENESIN. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does DEXTROMETHORPHAN\GUAIFENESIN Cause?
Drug ineffective (64)
Dizziness (48)
Wrong technique in product usage process (44)
Diarrhoea (41)
Nausea (33)
Product size issue (29)
Feeling abnormal (28)
Vomiting (22)
Extra dose administered (21)
Serotonin syndrome (19)
What Other Drugs Cause Product use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which DEXTROMETHORPHAN\GUAIFENESIN Alternatives Have Lower Product use complaint Risk?
DEXTROMETHORPHAN\GUAIFENESIN vs DEXTROSE
DEXTROMETHORPHAN\GUAIFENESIN vs DEXTROSE\DEXTROSE
DEXTROMETHORPHAN\GUAIFENESIN vs DEXTROSE\DEXTROSE\DOBUTAMINE\DOBUTAMINE
DEXTROMETHORPHAN\GUAIFENESIN vs DEXTROSE\HEPARIN
DEXTROMETHORPHAN\GUAIFENESIN vs DEXTROSE\LIDOCAINE