CHLORDIAZEPOXIDE HYDROCHLORIDE

N/A

Manufactured by Chartwell RX, LLC

267 FDA adverse event reports analyzed

Last updated: 2026-04-15

About CHLORDIAZEPOXIDE HYDROCHLORIDE

CHLORDIAZEPOXIDE HYDROCHLORIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Chartwell RX, LLC. The most commonly reported adverse reactions for CHLORDIAZEPOXIDE HYDROCHLORIDE include DRUG INEFFECTIVE, DIZZINESS, FATIGUE, HEADACHE, BACK PAIN. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CHLORDIAZEPOXIDE HYDROCHLORIDE.

Top Adverse Reactions

DRUG INEFFECTIVE10 reports
DIZZINESS9 reports
FATIGUE9 reports
HEADACHE6 reports
BACK PAIN5 reports
COMPLETED SUICIDE5 reports
DIARRHOEA5 reports
DRY MOUTH5 reports
DYSPNOEA5 reports
NAUSEA5 reports
SOMNOLENCE5 reports
TOXICITY TO VARIOUS AGENTS5 reports
ACUTE KIDNEY INJURY4 reports
ANXIETY4 reports
ASTHENIA4 reports
BLOOD PRESSURE INCREASED4 reports
CONFUSIONAL STATE4 reports
DYSPEPSIA4 reports
MALAISE4 reports
OFF LABEL USE4 reports
OVERDOSE4 reports
PAIN4 reports
PRODUCT QUALITY ISSUE4 reports
VOMITING4 reports
BLOOD GLUCOSE INCREASED3 reports
DEATH3 reports
DEMENTIA3 reports
DRUG ABUSE3 reports
DRUG DEPENDENCE3 reports
ERECTILE DYSFUNCTION3 reports
HOT FLUSH3 reports
INTENTIONAL PRODUCT MISUSE3 reports
MIGRAINE3 reports
PLATELET COUNT DECREASED3 reports
SEIZURE3 reports
TINNITUS3 reports
ACCIDENTAL OVERDOSE2 reports
ADVERSE EVENT2 reports
ALCOHOLISM2 reports
ALTERED STATE OF CONSCIOUSNESS2 reports
BLADDER CANCER2 reports
BLOOD CHOLESTEROL INCREASED2 reports
CHRONIC OBSTRUCTIVE PULMONARY DISEASE2 reports
COUGH2 reports
DEHYDRATION2 reports
DEPRESSION2 reports
DRUG ADMINISTRATION ERROR2 reports
DRUG HYPERSENSITIVITY2 reports
DRUG WITHDRAWAL SYNDROME2 reports
DYSSTASIA2 reports
ECZEMA2 reports
FALL2 reports
FEELING ABNORMAL2 reports
GASTROINTESTINAL DISORDER2 reports
HOSPITALISATION2 reports
HYPERTENSION2 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION2 reports
INCORRECT DOSE ADMINISTERED2 reports
INJECTION SITE PRURITUS2 reports
INJECTION SITE RASH2 reports
INSOMNIA2 reports
LOSS OF CONSCIOUSNESS2 reports
MUSCULAR WEAKNESS2 reports
NEUROPATHY PERIPHERAL2 reports
NIGHTMARE2 reports
PAIN IN EXTREMITY2 reports
PANCYTOPENIA2 reports
PARAESTHESIA2 reports
PARKINSONISM2 reports
POISONING2 reports
POLLAKIURIA2 reports
PRODUCT DOSE OMISSION ISSUE2 reports
PRURITUS2 reports
RESPIRATORY ARREST2 reports
SKIN EXFOLIATION2 reports
UNRESPONSIVE TO STIMULI2 reports
URINARY TRACT INFECTION2 reports
VISION BLURRED2 reports
WEIGHT DECREASED2 reports
WEIGHT INCREASED2 reports
WITHDRAWAL SYNDROME2 reports
ABDOMINAL DISCOMFORT1 reports
ABDOMINAL PAIN1 reports
ABDOMINAL PAIN UPPER1 reports
ACUTE RESPIRATORY FAILURE1 reports
ADVERSE DRUG REACTION1 reports
AGITATION1 reports
ALANINE AMINOTRANSFERASE INCREASED1 reports
ALCOHOL ABUSE1 reports
ALLERGY TO METALS1 reports
ANORECTAL DISORDER1 reports
ANORECTAL VARICES1 reports
ANTICHOLINERGIC SYNDROME1 reports
ARTERIOSCLEROSIS1 reports
ARTHRITIS1 reports
ASCITES1 reports
ASPARTATE AMINOTRANSFERASE INCREASED1 reports
ATRIAL FIBRILLATION1 reports
ATRIAL THROMBOSIS1 reports
BALANCE DISORDER1 reports

Report Outcomes

Out of 102 classified reports for CHLORDIAZEPOXIDE HYDROCHLORIDE:

Serious 61.8%Non-Serious 38.2%

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

Female60 (61.2%)
Male37 (37.8%)
Unknown1 (1.0%)

Reports by Age

Age 596 reports
Age 514 reports
Age 564 reports
Age 774 reports
Age 443 reports
Age 693 reports
Age 713 reports
Age 783 reports
Age 833 reports
Age 252 reports
Age 522 reports
Age 632 reports
Age 642 reports
Age 672 reports
Age 762 reports
Age 802 reports
Age 912 reports
Age 231 reports
Age 301 reports
Age 331 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 CHLORDIAZEPOXIDE HYDROCHLORIDE?

This profile reflects 267 FDA FAERS reports that mention CHLORDIAZEPOXIDE HYDROCHLORIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for CHLORDIAZEPOXIDE HYDROCHLORIDE?

Frequently reported terms in FAERS include DRUG INEFFECTIVE, DIZZINESS, FATIGUE, HEADACHE, BACK PAIN, COMPLETED SUICIDE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures CHLORDIAZEPOXIDE HYDROCHLORIDE?

Labeling and FAERS entries often list Chartwell RX, LLC in connection with CHLORDIAZEPOXIDE HYDROCHLORIDE. 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.