Does GUAIFENESIN Cause Product complaint? 34 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 34 reports of Product complaint have been filed in association with GUAIFENESIN (Guaifenesin and Pseudoephedrine HCl). This represents 0.4% of all adverse event reports for GUAIFENESIN.
34
Reports of Product complaint with GUAIFENESIN
0.4%
of all GUAIFENESIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product complaint From GUAIFENESIN?
Of the 34 reports, and 1 (2.9%) were considered life-threatening.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUAIFENESIN. However, 34 reports have been filed with the FAERS database.
What Other Side Effects Does GUAIFENESIN Cause?
Drug ineffective (1,583)
Incorrect drug administration duration (490)
No adverse event (462)
Product use in unapproved indication (451)
Dizziness (423)
Accidental overdose (396)
Diarrhoea (359)
Nausea (344)
Headache (308)
Product use issue (290)
What Other Drugs Cause Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
Which GUAIFENESIN Alternatives Have Lower Product complaint Risk?
GUAIFENESIN vs GUAIFENESIN\HYDROCODONE
GUAIFENESIN vs GUAIFENESIN\PSEUDOEPHEDRINE
GUAIFENESIN vs GUANFACINE
GUAIFENESIN vs GUSELKUMAB
GUAIFENESIN vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX