Does CHLORHEXIDINE Cause Recalled product? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Recalled product have been filed in association with CHLORHEXIDINE (Dyna-Hex 2). This represents 0.3% of all adverse event reports for CHLORHEXIDINE.
28
Reports of Recalled product with CHLORHEXIDINE
0.3%
of all CHLORHEXIDINE reports
4
Deaths
0
Hospitalizations
How Dangerous Is Recalled product From CHLORHEXIDINE?
Of the 28 reports, 4 (14.3%) resulted in death.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CHLORHEXIDINE. However, 28 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?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
ALCOHOL (26)
LEVOTHYROXINE (24)
Which CHLORHEXIDINE Alternatives Have Lower Recalled product Risk?
CHLORHEXIDINE vs CHLORHEXIDINE\CHLORHEXIDINE
CHLORHEXIDINE vs CHLORHEXIDINE\ISOPROPYL ALCOHOL
CHLORHEXIDINE vs CHLORMADINONE
CHLORHEXIDINE vs CHLORMEZANONE
CHLORHEXIDINE vs CHLOROQUINE