DrugCite
Search

CHLORHEXIDINE GLUCONATE

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Chlorhexidine Gluconate Adverse Events Reported to the FDA Over Time

How are Chlorhexidine Gluconate adverse event reports trending over time?

This graph shows volume of adverse events submitted to the FDA by quarter for Chlorhexidine Gluconate, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Chlorhexidine Gluconate is flagged as the suspect drug causing the adverse event.

Most Common Chlorhexidine Gluconate Adverse Events Reported to the FDA

What are the most common Chlorhexidine Gluconate adverse events reported to the FDA?

Anaphylactic Reaction
63 (4.05%)
Erythema
27 (1.74%)
Urticaria
27 (1.74%)
Burkholderia Cepacia Infection
26 (1.67%)
Hypotension
26 (1.67%)
Eye Inflammation
23 (1.48%)
Cardiac Failure Congestive
20 (1.29%)
Chronic Obstructive Pulmonary Disea...
19 (1.22%)
Anaphylactic Shock
17 (1.09%)
Cleft Lip And Palate
17 (1.09%)
Pruritus
17 (1.09%)
Show More Show More
Rash
17 (1.09%)
Dyspnoea
16 (1.03%)
Tachycardia
15 (.96%)
Blister
14 (.9%)
Dizziness
14 (.9%)
Hypersensitivity
14 (.9%)
Medication Error
14 (.9%)
Burning Sensation
13 (.84%)
Maternal Condition Affecting Foetus
12 (.77%)
Accidental Exposure
11 (.71%)
Ageusia
11 (.71%)
Caustic Injury
11 (.71%)
Dysgeusia
11 (.71%)
Swelling Face
11 (.71%)
Teratogenicity
11 (.71%)
Vomiting
11 (.71%)
Circulatory Collapse
10 (.64%)
Cystitis
10 (.64%)
Incorrect Route Of Drug Administrat...
10 (.64%)
Bacteraemia
9 (.58%)
Drug Hypersensitivity
9 (.58%)
Oxygen Saturation Decreased
9 (.58%)
Product Quality Issue
9 (.58%)
Rash Erythematous
9 (.58%)
Application Site Erythema
8 (.51%)
Application Site Reaction
8 (.51%)
Catheter Related Infection
8 (.51%)
Feeling Abnormal
8 (.51%)
Infection
8 (.51%)
Maternal Drugs Affecting Foetus
8 (.51%)
Pain
8 (.51%)
Pyrexia
8 (.51%)
Rash Pruritic
8 (.51%)
Skin Exfoliation
8 (.51%)
Skin Irritation
8 (.51%)
Swollen Tongue
8 (.51%)
Transmission Of An Infectious Agent...
8 (.51%)
Vulvovaginal Burning Sensation
8 (.51%)
Blood Pressure Decreased
7 (.45%)
Drug Exposure During Pregnancy
7 (.45%)
Excoriation
7 (.45%)
Flushing
7 (.45%)
Lip Swelling
7 (.45%)
Respiratory Failure
7 (.45%)
Skin Disorder
7 (.45%)
Skin Reaction
7 (.45%)
Tryptase Increased
7 (.45%)
Blood Disorder
6 (.39%)
Cleft Lip
6 (.39%)
Cleft Palate
6 (.39%)
Congenital Anomaly
6 (.39%)
Culture Positive
6 (.39%)
Emotional Disorder
6 (.39%)
Malaise
6 (.39%)
Nausea
6 (.39%)
Oral Discomfort
6 (.39%)
Sputum Culture Positive
6 (.39%)
Wrong Drug Administered
6 (.39%)
Abortion Induced
5 (.32%)
Blood Culture Positive
5 (.32%)
Cardiac Arrest
5 (.32%)
Convulsion
5 (.32%)
Diarrhoea
5 (.32%)
Eustachian Tube Dysfunction
5 (.32%)
Glossodynia
5 (.32%)
Hydrocele
5 (.32%)
Loss Of Consciousness
5 (.32%)
Oedema
5 (.32%)
Oedema Peripheral
5 (.32%)
Off Label Use
5 (.32%)
Otitis Media Chronic
5 (.32%)
Post Procedural Complication
5 (.32%)
Renal Failure
5 (.32%)
Sepsis
5 (.32%)
Throat Tightness
5 (.32%)
Abortion
4 (.26%)
Bronchospasm
4 (.26%)
Chills
4 (.26%)
Condition Aggravated
4 (.26%)
Cough
4 (.26%)
Cytolytic Hepatitis
4 (.26%)
Dermatitis Exfoliative
4 (.26%)
Eye Irritation
4 (.26%)
Eye Pain
4 (.26%)
Haemorrhage
4 (.26%)
Klebsiella Infection
4 (.26%)
Labile Blood Pressure
4 (.26%)
Necrosis
4 (.26%)
Oedema Mouth
4 (.26%)
Oral Disorder
4 (.26%)

ExportShare/Embed GraphExport Export Data

This graph shows the top adverse events submitted to the FDA for Chlorhexidine Gluconate, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Chlorhexidine Gluconate is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Adverse Event Categories for Chlorhexidine Gluconate

What are the most common Chlorhexidine Gluconate adverse events reported to the FDA?

Show More Show More

ExportShare/Embed Graph Export Export Data

This graph shows the top categories of adverse events submitted to the FDA for Chlorhexidine Gluconate, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Chlorhexidine Gluconate is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Common Uses of Chlorhexidine Gluconate According to Those Reporting Adverse Events

Why are people taking Chlorhexidine Gluconate, according to those reporting adverse events to the FDA?

Product Used For Unknown Indication
129
Drug Use For Unknown Indication
120
Preoperative Care
63
Infection Prophylaxis
50
Gingivitis
49
Prophylaxis
38
Show More Show More
Antibiotic Prophylaxis
26
Mucosal Inflammation
24
Folliculitis
16
Anti-infective Therapy
15
Stomatitis
13
Dental Care
11
Surgery
11
Oral Disorder
10
Postoperative Wound Infection
9
Dental Disorder Prophylaxis
8
Periodontal Disease
8
Local Anaesthesia
8
Periodontitis
7
Local Antibacterial Therapy
6
Antibiotic Therapy
6
Acanthamoeba Keratitis
6
Foetal Exposure During Pregnancy
6
Therapeutic Procedure
5
Oral Surgery
5
Oral Infection
5
Dry Mouth
4
Alveolar Osteitis
4
Tongue Geographic
4
Oral Fungal Infection
3
Skin Disorder
3
Bacterial Infection
3
Anaesthesia
3
Dental Plaque
3
Tooth Extraction
3
Gastrointestinal Disorder Therapy
3
Postoperative Care
3
Oropharyngeal Pain
3
Antibacterial Prophylaxis
3
Staphylococcal Infection
3
Subcutaneous Abscess
3
Drug Exposure During Pregnancy
3
Mouth Ulceration
3
Maternal Exposure During Pregnancy
3
Oral Discomfort
3
Tonsillitis
3
Tongue Ulceration
3
Abdominal Pain
2
Accidental Exposure
2
Knee Arthroplasty
2
Oral Candidiasis
2

Drug Labels

LabelLabelerEffective
Chlorhexidine GluconateAtlantic Biologicals Corps01-AUG-09
Chlorhexidine GluconateAtlantic Biologicals Corps01-AUG-09
Chlorhexidine GluconatePhysicians Total Care, Inc.24-FEB-10
Chlorhexidine GluconateXttrium Laboratories, Inc.24-FEB-10
PeriochipAdrian Pharmaceuticals, LLC05-MAR-10
PeriogardColgate-Palmolive Company05-MAR-10
Denti-care Denti-rinsechlorhexidine Gluconate Oral RinseAR Medicom Inc.28-APR-10
Chlorhexidine GluconateZila Therapeutics30-APR-10
Superdentchlorhexidine Gluconate Oral RinseDarby Dental Supply Co Inc20-MAY-10
Aplicare Antiseptic Chlorhexidine GluconateAplicare, Inc.09-JUN-10
Aplicare Antiseptic Chlorhexidine GluconateAplicare, Inc.29-JUN-10
Chlorhexidine GluconateRebel Distributors Corp23-SEP-10
HibiclensMolnlycke Health Care US, LLC12-JAN-11
HibistatMolnlycke Health Care US, LLC19-APR-11
Chlorhexidine GluconateMedline Industries, Inc.16-AUG-11
Chlorhexidine GluconateSunstar Americas, Inc.03-NOV-11
Chlorhexidine GluconateSage Products Inc.20-JUN-12
HibiclensPhysicians Total Care, Inc.19-SEP-12
Skin Antisepsis, Oral Cleansing, Nasal AntisepsisSage Products, Inc.22-OCT-12
Bactoshield ChgSTERIS Corporation05-DEC-12
Antiseptic Skin CleanserAVA, Inc.06-DEC-12
Antiseptic Skin CleanserAVA, Inc.16-DEC-12
Bactoshield ChgSTERIS Corporation09-JAN-13
Peridex3M ESPE Dental Products25-JAN-13
BactoshieldSTERIS Corporation18-MAR-13
Chlorhexidine GluconateHi-Tech Pharmacal Co., Inc.23-MAR-13
Skin Antisepsis, Oral Cleansing, Nasal AntisepsisSage Products, Inc.02-APR-13

Chlorhexidine Gluconate Case Reports

What Chlorhexidine Gluconate safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Chlorhexidine Gluconate. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.

DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.

DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.

Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.

Comments

Share your experience with Chlorhexidine Gluconate.