WITCH HAZEL

N/A

Manufactured by Haleon US Holdings LLC

488 FDA adverse event reports analyzed

Last updated: 2026-04-15

About WITCH HAZEL

WITCH HAZEL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Haleon US Holdings LLC. The most commonly reported adverse reactions for WITCH HAZEL include DRUG INEFFECTIVE, HEADACHE, NAUSEA, ERYTHEMA, RECTAL HAEMORRHAGE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for WITCH HAZEL.

Top Adverse Reactions

DRUG INEFFECTIVE14 reports
HEADACHE14 reports
NAUSEA13 reports
ERYTHEMA12 reports
RECTAL HAEMORRHAGE11 reports
FATIGUE10 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION10 reports
PAIN10 reports
SINUSITIS10 reports
SKIN BURNING SENSATION10 reports
DIARRHOEA9 reports
PRODUCT DOSE OMISSION ISSUE9 reports
PRODUCT USE ISSUE9 reports
CONDITION AGGRAVATED8 reports
COVID 198 reports
RASH8 reports
VOMITING8 reports
DECREASED APPETITE7 reports
DRY SKIN7 reports
ILLNESS7 reports
INSURANCE ISSUE7 reports
MALAISE7 reports
PNEUMONIA7 reports
DIZZINESS6 reports
DYSPNOEA6 reports
HAEMORRHOIDS6 reports
PRURITUS6 reports
UPPER RESPIRATORY TRACT INFECTION6 reports
ACNE5 reports
ASTHENIA5 reports
BURNING SENSATION5 reports
CONTUSION5 reports
FALL5 reports
FEBRILE NEUTROPENIA5 reports
HAEMORRHAGE5 reports
INFECTION5 reports
NASOPHARYNGITIS5 reports
OFF LABEL USE5 reports
OROPHARYNGEAL PAIN5 reports
PRODUCT USE IN UNAPPROVED INDICATION5 reports
PYREXIA5 reports
WEIGHT DECREASED5 reports
WEIGHT INCREASED5 reports
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS5 reports
ABDOMINAL PAIN4 reports
ARTHRALGIA4 reports
ASTHMA4 reports
HYPERSENSITIVITY4 reports
PRODUCT PHYSICAL ISSUE4 reports
SKIN IRRITATION4 reports
TOOTH INFECTION4 reports
URINARY TRACT INFECTION4 reports
VISION BLURRED4 reports
ACUTE KIDNEY INJURY3 reports
ANAL FISSURE3 reports
ASPARTATE AMINOTRANSFERASE INCREASED3 reports
BACK PAIN3 reports
BLOOD PRESSURE INCREASED3 reports
BRONCHITIS3 reports
CANDIDA INFECTION3 reports
CELLULITIS3 reports
CEREBROVASCULAR ACCIDENT3 reports
CONSTIPATION3 reports
COUGH3 reports
CREUTZFELDT JAKOB DISEASE3 reports
DEATH3 reports
DISCOMFORT3 reports
DRUG HYPERSENSITIVITY3 reports
EAR INFECTION3 reports
HAEMORRHOIDAL HAEMORRHAGE3 reports
HYPERBILIRUBINAEMIA3 reports
HYPERTENSION3 reports
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION3 reports
INFLUENZA3 reports
INFUSION SITE EXTRAVASATION3 reports
INJECTION SITE PAIN3 reports
MEMORY IMPAIRMENT3 reports
MIGRAINE3 reports
PLEURAL EFFUSION3 reports
POOR QUALITY DRUG ADMINISTERED3 reports
PRODUCT QUALITY ISSUE3 reports
RASH MACULAR3 reports
SKIN EXFOLIATION3 reports
SWELLING3 reports
THROMBOCYTOPENIA3 reports
TOOTH DISORDER3 reports
ABDOMINAL DISTENSION2 reports
ACROCHORDON2 reports
ALANINE AMINOTRANSFERASE INCREASED2 reports
ANXIETY2 reports
APPLICATION SITE PAIN2 reports
ATRIAL FIBRILLATION2 reports
BLISTER2 reports
BLOOD URINE PRESENT2 reports
CARDIAC FAILURE ACUTE2 reports
CARDIAC FAILURE CONGESTIVE2 reports
CHILLS2 reports
CHRONIC KIDNEY DISEASE2 reports
COLITIS ULCERATIVE2 reports
CORONARY ARTERY DISEASE2 reports

Report Outcomes

Out of 163 classified reports for WITCH HAZEL:

Serious 71.2%Non-Serious 28.8%

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

Female105 (66.9%)
Male52 (33.1%)

Reports by Age

Age 526 reports
Age 546 reports
Age 586 reports
Age 695 reports
Age 574 reports
Age 604 reports
Age 644 reports
Age 654 reports
Age 463 reports
Age 593 reports
Age 613 reports
Age 663 reports
Age 743 reports
Age 873 reports
Age 152 reports
Age 172 reports
Age 202 reports
Age 292 reports
Age 342 reports
Age 392 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 WITCH HAZEL?

This profile reflects 488 FDA FAERS reports that mention WITCH HAZEL. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for WITCH HAZEL?

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

Who manufactures WITCH HAZEL?

Labeling and FAERS entries often list Haleon US Holdings LLC in connection with WITCH HAZEL. 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.