ACETIC ACID

N/A

Manufactured by B. Braun Medical Inc.

953 FDA adverse event reports analyzed

Last updated: 2026-04-15

About ACETIC ACID

ACETIC ACID is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by B. Braun Medical Inc.. The most commonly reported adverse reactions for ACETIC ACID include NAUSEA, DIARRHOEA, TOXICITY TO VARIOUS AGENTS, PAIN, ARTHRALGIA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ACETIC ACID.

Top Adverse Reactions

NAUSEA35 reports
DIARRHOEA29 reports
TOXICITY TO VARIOUS AGENTS28 reports
PAIN22 reports
ARTHRALGIA20 reports
DRUG INEFFECTIVE20 reports
OFF LABEL USE20 reports
COUGH18 reports
DIZZINESS18 reports
ANAEMIA16 reports
DYSPNOEA16 reports
FATIGUE16 reports
MALAISE16 reports
RASH16 reports
DEPRESSION15 reports
CONSTIPATION14 reports
CORONARY ARTERY DISEASE14 reports
ERYTHEMA13 reports
ABDOMINAL PAIN12 reports
HEADACHE12 reports
NASOPHARYNGITIS12 reports
PYREXIA12 reports
ANXIETY11 reports
CARDIAC DISORDER11 reports
DEATH11 reports
DYSPHONIA11 reports
MUSCLE SPASMS11 reports
PAIN IN EXTREMITY11 reports
URINARY TRACT INFECTION11 reports
CHRONIC KIDNEY DISEASE10 reports
PRURITUS10 reports
VOMITING10 reports
WEIGHT DECREASED10 reports
FALL9 reports
GAIT DISTURBANCE9 reports
OBSTRUCTIVE AIRWAYS DISORDER9 reports
PSORIASIS9 reports
WHEEZING9 reports
ATRIAL FIBRILLATION8 reports
COLITIS8 reports
HYPERTENSION8 reports
PNEUMONIA8 reports
SECRETION DISCHARGE8 reports
ADVERSE DRUG REACTION7 reports
BACK PAIN7 reports
BRAIN NATRIURETIC PEPTIDE INCREASED7 reports
CHEST DISCOMFORT7 reports
CHRONIC SINUSITIS7 reports
DYSPEPSIA7 reports
DYSPNOEA EXERTIONAL7 reports
EAR DISCOMFORT7 reports
EOSINOPHILIA7 reports
FRACTIONAL EXHALED NITRIC OXIDE INCREASED7 reports
ILLNESS7 reports
INSOMNIA7 reports
JOINT SWELLING7 reports
MULTIPLE ORGAN DYSFUNCTION SYNDROME7 reports
MYOGLOBIN BLOOD INCREASED7 reports
OBSTRUCTIVE SLEEP APNOEA SYNDROME7 reports
ORAL CANDIDIASIS7 reports
PARAESTHESIA ORAL7 reports
PLANTAR FASCIITIS7 reports
RADICULOPATHY7 reports
SWELLING FACE7 reports
THERAPEUTIC PRODUCT EFFECT INCOMPLETE7 reports
UPPER GASTROINTESTINAL HAEMORRHAGE7 reports
ACUTE KIDNEY INJURY6 reports
CHEST PAIN6 reports
COLITIS ULCERATIVE6 reports
EXOSTOSIS6 reports
FEMALE GENITAL TRACT FISTULA6 reports
FREQUENT BOWEL MOVEMENTS6 reports
HAEMATOCHEZIA6 reports
HYPERSENSITIVITY6 reports
INFUSION RELATED REACTION6 reports
LIP SWELLING6 reports
MACULAR DEGENERATION6 reports
MEDICATION ERROR6 reports
MEMORY IMPAIRMENT6 reports
MUSCULAR WEAKNESS6 reports
MYALGIA6 reports
NEURALGIA6 reports
OEDEMA PERIPHERAL6 reports
PNEUMOTHORAX6 reports
PROCEDURAL PAIN6 reports
PROCTITIS6 reports
RECTAL HAEMORRHAGE6 reports
RENAL FAILURE6 reports
SENSATION OF FOREIGN BODY6 reports
STRESS6 reports
VAGINAL DISCHARGE6 reports
VAGINAL FLATULENCE6 reports
ABDOMINAL PAIN UPPER5 reports
CHRONIC OBSTRUCTIVE PULMONARY DISEASE5 reports
CONDITION AGGRAVATED5 reports
DECREASED APPETITE5 reports
EAR PAIN5 reports
END STAGE RENAL DISEASE5 reports
HEART RATE INCREASED5 reports
INFECTION5 reports

Report Outcomes

Out of 325 classified reports for ACETIC ACID:

Serious 78.5%Non-Serious 21.5%

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

Female197 (65.9%)
Male101 (33.8%)
Unknown1 (0.3%)

Reports by Age

Age 5221 reports
Age 6612 reports
Age 7711 reports
Age 5110 reports
Age 409 reports
Age 639 reports
Age 719 reports
Age 568 reports
Age 287 reports
Age 597 reports
Age 627 reports
Age 695 reports
Age 745 reports
Age 504 reports
Age 544 reports
Age 604 reports
Age 644 reports
Age 654 reports
Age 724 reports
Age 734 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 ACETIC ACID?

This profile reflects 953 FDA FAERS reports that mention ACETIC ACID. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for ACETIC ACID?

Frequently reported terms in FAERS include NAUSEA, DIARRHOEA, TOXICITY TO VARIOUS AGENTS, PAIN, ARTHRALGIA, DRUG INEFFECTIVE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures ACETIC ACID?

Labeling and FAERS entries often list B. Braun Medical Inc. in connection with ACETIC ACID. 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.