HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK

N/A

Manufactured by Boiron

1,361 FDA adverse event reports analyzed

Last updated: 2026-04-15

About HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK

HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Boiron. The most commonly reported adverse reactions for HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK include IMPAIRED HEALING, GASTROINTESTINAL DISORDER, HEADACHE, ILL-DEFINED DISORDER, ALOPECIA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK.

Top Adverse Reactions

IMPAIRED HEALING18 reports
GASTROINTESTINAL DISORDER17 reports
HEADACHE17 reports
ILL DEFINED DISORDER17 reports
ALOPECIA16 reports
FATIGUE16 reports
GLOSSODYNIA16 reports
GRIP STRENGTH DECREASED16 reports
HYPERSENSITIVITY16 reports
HYPERTENSION16 reports
PAIN16 reports
CONTUSION15 reports
DECREASED APPETITE15 reports
DYSPNOEA15 reports
GENERAL PHYSICAL HEALTH DETERIORATION15 reports
HAND DEFORMITY15 reports
HELICOBACTER INFECTION15 reports
HEPATIC ENZYME INCREASED15 reports
HYPERCHOLESTEROLAEMIA15 reports
INFECTION15 reports
ADJUSTMENT DISORDER WITH DEPRESSED MOOD14 reports
AMNESIA14 reports
BREAST CANCER STAGE II14 reports
CHEST PAIN14 reports
DELIRIUM14 reports
DIARRHOEA14 reports
DISCOMFORT14 reports
DISLOCATION OF VERTEBRA14 reports
FOLLICULITIS14 reports
INJURY14 reports
IRRITABLE BOWEL SYNDROME14 reports
LOWER RESPIRATORY TRACT INFECTION14 reports
MALAISE14 reports
MUSCLE INJURY14 reports
OEDEMA14 reports
PERICARDITIS14 reports
PERIPHERAL SWELLING14 reports
PRURITUS14 reports
PSORIATIC ARTHROPATHY14 reports
PULMONARY FIBROSIS14 reports
PYREXIA14 reports
RASH14 reports
ABDOMINAL DISCOMFORT13 reports
ABDOMINAL PAIN UPPER13 reports
ANTI CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE13 reports
ARTHRALGIA13 reports
ARTHROPATHY13 reports
BACK DISORDER13 reports
BLISTER13 reports
BLOOD CHOLESTEROL INCREASED13 reports
CONDITION AGGRAVATED13 reports
CONFUSIONAL STATE13 reports
DEPRESSION13 reports
DRUG HYPERSENSITIVITY13 reports
DUODENAL ULCER PERFORATION13 reports
DYSPEPSIA13 reports
FIBROMYALGIA13 reports
FLUID RETENTION13 reports
GAIT DISTURBANCE13 reports
GAIT INABILITY13 reports
GENERAL SYMPTOM13 reports
HYPOAESTHESIA13 reports
INFUSION RELATED REACTION13 reports
JOINT RANGE OF MOTION DECREASED13 reports
JOINT SWELLING13 reports
LIVER INJURY13 reports
MEMORY IMPAIRMENT13 reports
MIGRAINE13 reports
MOBILITY DECREASED13 reports
MUSCULOSKELETAL STIFFNESS13 reports
MYOSITIS13 reports
NASOPHARYNGITIS13 reports
NAUSEA13 reports
PAIN IN EXTREMITY13 reports
PEMPHIGUS13 reports
PNEUMONIA13 reports
PSORIASIS13 reports
PUSTULAR PSORIASIS13 reports
RASH VESICULAR13 reports
RHEUMATIC FEVER13 reports
SINUSITIS13 reports
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE13 reports
STOMATITIS13 reports
SYSTEMIC LUPUS ERYTHEMATOSUS13 reports
URTICARIA13 reports
RHEUMATOID ARTHRITIS12 reports
RHEUMATOID FACTOR POSITIVE12 reports
SLEEP DISORDER12 reports
SUBCUTANEOUS DRUG ABSORPTION IMPAIRED12 reports
SWELLING12 reports
SWOLLEN JOINT COUNT INCREASED12 reports
SYNOVITIS12 reports
TYPE 2 DIABETES MELLITUS12 reports
VOMITING12 reports
WALKING AID USER12 reports
WEIGHT DECREASED12 reports
WEIGHT INCREASED12 reports
WHEEZING12 reports
DISABILITY11 reports
HIP ARTHROPLASTY11 reports

Report Outcomes

Out of 37 classified reports for HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK:

Serious 83.8%Non-Serious 16.2%

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

Female26 (86.7%)
Male4 (13.3%)

Reports by Age

Age 9712 reports
Age 432 reports
Age 472 reports
Age 451 reports
Age 531 reports
Age 591 reports
Age 611 reports
Age 651 reports
Age 701 reports
Age 721 reports
Age 751 reports
Age 771 reports
Age 811 reports
Age 961 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 HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK?

This profile reflects 1,361 FDA FAERS reports that mention HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK?

Frequently reported terms in FAERS include IMPAIRED HEALING, GASTROINTESTINAL DISORDER, HEADACHE, ILL-DEFINED DISORDER, ALOPECIA, FATIGUE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK?

Labeling and FAERS entries often list Boiron in connection with HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK. 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.