Does CETRIMIDE\CHLORHEXIDINE Cause Product use issue? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product use issue have been filed in association with CETRIMIDE\CHLORHEXIDINE. This represents 29.6% of all adverse event reports for CETRIMIDE\CHLORHEXIDINE.
13
Reports of Product use issue with CETRIMIDE\CHLORHEXIDINE
29.6%
of all CETRIMIDE\CHLORHEXIDINE reports
9
Deaths
12
Hospitalizations
How Dangerous Is Product use issue From CETRIMIDE\CHLORHEXIDINE?
Of the 13 reports, 9 (69.2%) resulted in death, 12 (92.3%) required hospitalization, and 10 (76.9%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CETRIMIDE\CHLORHEXIDINE. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does CETRIMIDE\CHLORHEXIDINE Cause?
Duodenal ulcer perforation (30)
Folliculitis (30)
Helicobacter infection (30)
Confusional state (28)
Drug ineffective (28)
Impaired healing (28)
Fatigue (27)
Gastrointestinal disorder (27)
Rheumatoid arthritis (27)
Stomatitis (27)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)