Does DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN Cause Expired product administered? 222 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 222 reports of Expired product administered have been filed in association with DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN. This represents 3.3% of all adverse event reports for DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN.
222
Reports of Expired product administered with DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN
3.3%
of all DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN reports
0
Deaths
6
Hospitalizations
How Dangerous Is Expired product administered From DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN?
Of the 222 reports, 6 (2.7%) required hospitalization.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN. However, 222 reports have been filed with the FAERS database.
What Other Side Effects Does DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN Cause?
Drug ineffective (1,155)
Dizziness (759)
Diarrhoea (570)
Accidental overdose (515)
Nausea (408)
Overdose (377)
Product use in unapproved indication (356)
Somnolence (304)
Insomnia (259)
Feeling abnormal (246)
What Other Drugs Cause Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
Which DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN Alternatives Have Lower Expired product administered Risk?
DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN vs DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN\PHENYLEPHRINE
DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN vs DEXTROMETHORPHAN HYDROBROMIDE\QUINIDINE
DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN vs DEXTROMETHORPHAN\GUAIFENESIN
DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN vs DEXTROSE
DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN vs DEXTROSE\DEXTROSE