Does CHLORHEXIDINE Cause Incorrect product administration duration? 64 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 64 reports of Incorrect product administration duration have been filed in association with CHLORHEXIDINE (Dyna-Hex 2). This represents 0.7% of all adverse event reports for CHLORHEXIDINE.
64
Reports of Incorrect product administration duration with CHLORHEXIDINE
0.7%
of all CHLORHEXIDINE reports
63
Deaths
62
Hospitalizations
How Dangerous Is Incorrect product administration duration From CHLORHEXIDINE?
Of the 64 reports, 63 (98.4%) resulted in death, 62 (96.9%) required hospitalization, and 62 (96.9%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CHLORHEXIDINE. However, 64 reports have been filed with the FAERS database.
What Other Side Effects Does CHLORHEXIDINE Cause?
Rash (3,921)
Joint swelling (3,779)
Fatigue (3,486)
Lower respiratory tract infection (3,485)
Pruritus (3,476)
Peripheral swelling (3,467)
Pain (3,463)
Hypersensitivity (3,453)
Folliculitis (3,405)
Impaired healing (3,341)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which CHLORHEXIDINE Alternatives Have Lower Incorrect product administration duration Risk?
CHLORHEXIDINE vs CHLORHEXIDINE\CHLORHEXIDINE
CHLORHEXIDINE vs CHLORHEXIDINE\ISOPROPYL ALCOHOL
CHLORHEXIDINE vs CHLORMADINONE
CHLORHEXIDINE vs CHLORMEZANONE
CHLORHEXIDINE vs CHLOROQUINE