HYDROGEN PEROXIDE

N/A

Manufactured by Rowpar Pharmaceuticals, Inc.

808 FDA adverse event reports analyzed

Last updated: 2026-04-15

About HYDROGEN PEROXIDE

HYDROGEN PEROXIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Rowpar Pharmaceuticals, Inc.. The most commonly reported adverse reactions for HYDROGEN PEROXIDE include DRUG INEFFECTIVE, NAUSEA, FATIGUE, PRURITUS, HEADACHE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for HYDROGEN PEROXIDE.

Top Adverse Reactions

DRUG INEFFECTIVE35 reports
NAUSEA24 reports
FATIGUE23 reports
PRURITUS17 reports
HEADACHE16 reports
VOMITING16 reports
RASH15 reports
PRODUCT USE IN UNAPPROVED INDICATION14 reports
SHOCK HAEMORRHAGIC14 reports
DYSPNOEA13 reports
GASTRITIS EROSIVE13 reports
PYREXIA13 reports
INTENTIONAL PRODUCT MISUSE12 reports
PARAESTHESIA12 reports
TOXICITY TO VARIOUS AGENTS12 reports
ASTHENIA11 reports
BACK PAIN10 reports
DIARRHOEA10 reports
GASTROINTESTINAL HAEMORRHAGE10 reports
HYPERSENSITIVITY10 reports
OFF LABEL USE10 reports
PRODUCT DOSE OMISSION ISSUE10 reports
ABDOMINAL PAIN UPPER9 reports
COUGH9 reports
DECREASED APPETITE9 reports
DIZZINESS9 reports
HYPOKALAEMIA9 reports
SYNCOPE9 reports
ARTHRALGIA8 reports
CELLULITIS8 reports
CHEMICAL INJURY8 reports
COMPLETED SUICIDE8 reports
CONDITION AGGRAVATED8 reports
FEBRILE NEUTROPENIA8 reports
ILLNESS8 reports
INJECTION SITE PAIN8 reports
MUSCLE SPASMS8 reports
PAIN8 reports
STOMATITIS8 reports
WHITE BLOOD CELL COUNT DECREASED8 reports
ABDOMINAL PAIN7 reports
ACUTE KIDNEY INJURY7 reports
COVID 197 reports
DRUG HYPERSENSITIVITY7 reports
FALL7 reports
GASTRIC ULCER7 reports
HYPERTENSION7 reports
HYPOAESTHESIA7 reports
HYPOTENSION7 reports
IMPAIRED HEALING7 reports
INFLUENZA LIKE ILLNESS7 reports
MALIGNANT NEOPLASM PROGRESSION7 reports
OSTEONECROSIS OF JAW7 reports
PAIN IN EXTREMITY7 reports
WEIGHT DECREASED7 reports
ABDOMINAL DISCOMFORT6 reports
ACCIDENTAL EXPOSURE TO PRODUCT6 reports
BLISTER6 reports
CARDIAC ARREST6 reports
CONTUSION6 reports
DEATH6 reports
FLUSHING6 reports
GAIT DISTURBANCE6 reports
INSOMNIA6 reports
LIP SWELLING6 reports
NASOPHARYNGITIS6 reports
OROPHARYNGEAL PAIN6 reports
PLATELET COUNT DECREASED6 reports
SUICIDE ATTEMPT6 reports
SWELLING6 reports
THERAPY NON RESPONDER6 reports
WHITE BLOOD CELL COUNT INCREASED6 reports
WOUND6 reports
ABDOMINAL DISTENSION5 reports
ANAEMIA5 reports
CHEST PAIN5 reports
DERMATITIS CONTACT5 reports
DYSPHAGIA5 reports
FEELING COLD5 reports
MIGRAINE5 reports
MULTIPLE ALLERGIES5 reports
OEDEMA5 reports
OVERDOSE5 reports
PNEUMONIA5 reports
PRODUCT USE ISSUE5 reports
RESPIRATORY ARREST5 reports
SINUSITIS5 reports
TREMOR5 reports
URINARY RETENTION5 reports
VISUAL IMPAIRMENT5 reports
ALANINE AMINOTRANSFERASE INCREASED4 reports
ATRIAL FIBRILLATION4 reports
BACTERIAL INFECTION4 reports
BLOOD PRESSURE INCREASED4 reports
BONE CANCER4 reports
BURNING SENSATION4 reports
CONFUSIONAL STATE4 reports
DRY MOUTH4 reports
DYSGEUSIA4 reports
DYSURIA4 reports

Report Outcomes

Out of 311 classified reports for HYDROGEN PEROXIDE:

Serious 77.8%Non-Serious 22.2%

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

Female140 (49.8%)
Male136 (48.4%)
Unknown5 (1.8%)

Reports by Age

Age 5420 reports
Age 5516 reports
Age 667 reports
Age 707 reports
Age 767 reports
Age 246 reports
Age 566 reports
Age 786 reports
Age 285 reports
Age 355 reports
Age 435 reports
Age 535 reports
Age 585 reports
Age 675 reports
Age 174 reports
Age 214 reports
Age 514 reports
Age 524 reports
Age 574 reports
Age 604 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 HYDROGEN PEROXIDE?

This profile reflects 808 FDA FAERS reports that mention HYDROGEN PEROXIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for HYDROGEN PEROXIDE?

Frequently reported terms in FAERS include DRUG INEFFECTIVE, NAUSEA, FATIGUE, PRURITUS, HEADACHE, VOMITING. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures HYDROGEN PEROXIDE?

Labeling and FAERS entries often list Rowpar Pharmaceuticals, Inc. in connection with HYDROGEN PEROXIDE. 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.