Does CHLORHEXIDINE Cause Recalled product administered? 47 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 47 reports of Recalled product administered have been filed in association with CHLORHEXIDINE (Dyna-Hex 2). This represents 0.5% of all adverse event reports for CHLORHEXIDINE.
47
Reports of Recalled product administered with CHLORHEXIDINE
0.5%
of all CHLORHEXIDINE reports
11
Deaths
10
Hospitalizations
How Dangerous Is Recalled product administered From CHLORHEXIDINE?
Of the 47 reports, 11 (23.4%) resulted in death, 10 (21.3%) required hospitalization, and 2 (4.3%) were considered life-threatening.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CHLORHEXIDINE. However, 47 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which CHLORHEXIDINE Alternatives Have Lower Recalled product administered Risk?
CHLORHEXIDINE vs CHLORHEXIDINE\CHLORHEXIDINE
CHLORHEXIDINE vs CHLORHEXIDINE\ISOPROPYL ALCOHOL
CHLORHEXIDINE vs CHLORMADINONE
CHLORHEXIDINE vs CHLORMEZANONE
CHLORHEXIDINE vs CHLOROQUINE