CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL

N/A

Manufactured by CareFusion 213 LLC

9,167 FDA adverse event reports analyzed

Last updated: 2026-04-15

About CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL

CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by CareFusion 213 LLC. The most commonly reported adverse reactions for CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL include SINUSITIS, PAIN, LOWER RESPIRATORY TRACT INFECTION, PRURITUS, RASH. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL.

Top Adverse Reactions

SINUSITIS210 reports
PAIN206 reports
LOWER RESPIRATORY TRACT INFECTION205 reports
PRURITUS191 reports
RASH187 reports
JOINT SWELLING186 reports
PERIPHERAL SWELLING181 reports
INSOMNIA179 reports
HYPERSENSITIVITY155 reports
IMPAIRED HEALING155 reports
FOLLICULITIS154 reports
STOMATITIS154 reports
WEIGHT INCREASED154 reports
BLISTER152 reports
FATIGUE152 reports
INFECTION152 reports
IRRITABLE BOWEL SYNDROME152 reports
PYREXIA152 reports
NASOPHARYNGITIS151 reports
CONFUSIONAL STATE150 reports
SWELLING149 reports
MUSCLE INJURY146 reports
GASTROINTESTINAL DISORDER145 reports
ARTHRALGIA142 reports
URTICARIA133 reports
DRUG INEFFECTIVE132 reports
DYSPNOEA129 reports
HEADACHE124 reports
VOMITING124 reports
CONTUSION122 reports
ILL DEFINED DISORDER122 reports
CONTRAINDICATED PRODUCT ADMINISTERED121 reports
NIGHT SWEATS118 reports
ASTHENIA114 reports
SLEEP DISORDER113 reports
DIARRHOEA112 reports
HELICOBACTER INFECTION110 reports
ABDOMINAL PAIN UPPER109 reports
EAR PAIN108 reports
HEPATIC ENZYME INCREASED106 reports
PERICARDITIS106 reports
INFUSION RELATED REACTION105 reports
MUSCLE SPASTICITY104 reports
PEMPHIGUS104 reports
SYNOVITIS104 reports
ALOPECIA103 reports
ANTI CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE103 reports
RESPIRATORY DISORDER103 reports
BACK PAIN101 reports
BODY TEMPERATURE INCREASED100 reports
ARTHROPATHY99 reports
SYSTEMIC LUPUS ERYTHEMATOSUS97 reports
THERAPEUTIC PRODUCT EFFECT DECREASED96 reports
GLOSSODYNIA95 reports
HAND DEFORMITY95 reports
ABDOMINAL DISCOMFORT94 reports
DUODENAL ULCER PERFORATION94 reports
DISCOMFORT91 reports
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE84 reports
OFF LABEL USE82 reports
DRUG INTOLERANCE75 reports
RHEUMATOID ARTHRITIS66 reports
WOUND61 reports
MEDICATION ERROR58 reports
INTENTIONAL PRODUCT USE ISSUE52 reports
PSORIATIC ARTHROPATHY47 reports
MATERNAL EXPOSURE DURING PREGNANCY44 reports
GENERAL PHYSICAL HEALTH DETERIORATION36 reports
HYPERTENSION35 reports
RHEUMATOID FACTOR POSITIVE35 reports
MUSCULOSKELETAL STIFFNESS34 reports
ABDOMINAL PAIN33 reports
INJURY33 reports
WHEEZING33 reports
CONDITION AGGRAVATED32 reports
TREATMENT FAILURE32 reports
TYPE 2 DIABETES MELLITUS32 reports
DRUG HYPERSENSITIVITY31 reports
JOINT RANGE OF MOTION DECREASED29 reports
MOBILITY DECREASED29 reports
NAUSEA29 reports
OEDEMA29 reports
LIP DRY28 reports
PREGNANCY28 reports
PRODUCT USE ISSUE28 reports
FIBROMYALGIA27 reports
INCORRECT ROUTE OF PRODUCT ADMINISTRATION27 reports
INFLAMMATION27 reports
RHEUMATIC FEVER27 reports
DRY MOUTH26 reports
LUNG DISORDER26 reports
OSTEOARTHRITIS26 reports
BLOOD CHOLESTEROL INCREASED25 reports
BURSITIS25 reports
HIP ARTHROPLASTY25 reports
DEPRESSION24 reports
DIZZINESS24 reports
HYPOAESTHESIA24 reports
KNEE ARTHROPLASTY24 reports
LIVER INJURY24 reports

Report Outcomes

Out of 300 classified reports for CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL:

Serious 91.0%Non-Serious 9.0%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Demographics Breakdown

Reports by Sex

Female234 (92.9%)
Male17 (6.7%)
Unknown1 (0.4%)

Reports by Age

Age 4249 reports
Age 4440 reports
Age 4526 reports
Age 434 reports
Age 563 reports
Age 142 reports
Age 272 reports
Age 402 reports
Age 462 reports
Age 472 reports
Age 552 reports
Age 582 reports
Age 652 reports
Age 31 reports
Age 91 reports
Age 101 reports
Age 301 reports
Age 371 reports
Age 481 reports
Age 511 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL?

This profile reflects 9,167 FDA FAERS reports that mention CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL?

Frequently reported terms in FAERS include SINUSITIS, PAIN, LOWER RESPIRATORY TRACT INFECTION, PRURITUS, RASH, JOINT SWELLING. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL?

Labeling and FAERS entries often list CareFusion 213 LLC in connection with CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL. Always verify the specific product and NDC with your pharmacist.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.