PANTHENOL

N/A

Manufactured by LAON COMMERCE co ltd

1,581 FDA adverse event reports analyzed

Last updated: 2026-04-15

About PANTHENOL

PANTHENOL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by LAON COMMERCE co ltd. The most commonly reported adverse reactions for PANTHENOL include NAUSEA, GENERAL PHYSICAL HEALTH DETERIORATION, CONDITION AGGRAVATED, DYSPNOEA, VOMITING. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for PANTHENOL.

Top Adverse Reactions

NAUSEA42 reports
GENERAL PHYSICAL HEALTH DETERIORATION37 reports
CONDITION AGGRAVATED31 reports
DYSPNOEA31 reports
VOMITING31 reports
ABDOMINAL PAIN30 reports
PYREXIA30 reports
ANAEMIA28 reports
DRY MOUTH27 reports
ASTHENIA23 reports
BLOOD CHOLESTEROL INCREASED23 reports
DIARRHOEA23 reports
OFF LABEL USE23 reports
PAIN23 reports
PNEUMONIA23 reports
SWELLING23 reports
SEPSIS20 reports
FATIGUE19 reports
HYPERSENSITIVITY19 reports
ASCITES18 reports
CONSTIPATION18 reports
DIZZINESS18 reports
DRUG INEFFECTIVE18 reports
SLEEP DISORDER18 reports
STOMATITIS18 reports
DRUG HYPERSENSITIVITY17 reports
OEDEMA PERIPHERAL17 reports
RASH17 reports
WEIGHT INCREASED17 reports
ABDOMINAL DISCOMFORT16 reports
ABDOMINAL PAIN UPPER16 reports
ALOPECIA16 reports
FIBROMYALGIA16 reports
MUSCULOSKELETAL STIFFNESS16 reports
ABDOMINAL DISTENSION15 reports
INTENTIONAL PRODUCT MISUSE15 reports
IRRITABLE BOWEL SYNDROME15 reports
SOMNOLENCE15 reports
WHEEZING15 reports
APPENDICITIS14 reports
DEATH14 reports
DECREASED APPETITE14 reports
DRUG INTOLERANCE14 reports
INCORRECT ROUTE OF PRODUCT ADMINISTRATION14 reports
LOWER RESPIRATORY TRACT INFECTION14 reports
OEDEMA14 reports
STRESS14 reports
APPENDICOLITH13 reports
ARTHRALGIA13 reports
BLOOD PHOSPHORUS INCREASED13 reports
CONFUSIONAL STATE13 reports
DIABETES MELLITUS13 reports
HYPONATRAEMIA13 reports
INFECTION13 reports
INJURY13 reports
IRON DEFICIENCY13 reports
LUNG DISORDER13 reports
MYASTHENIA GRAVIS13 reports
PARAESTHESIA13 reports
PERIPHERAL SWELLING13 reports
PULMONARY EMBOLISM13 reports
RHEUMATOID ARTHRITIS13 reports
SYNOVITIS13 reports
THROMBOSIS13 reports
URTICARIA13 reports
VENTRICULAR FIBRILLATION13 reports
BLOOD URIC ACID INCREASED12 reports
CARDIOGENIC SHOCK12 reports
CHRONIC OBSTRUCTIVE PULMONARY DISEASE12 reports
HEADACHE12 reports
HYPOTENSION12 reports
MULTIPLE ORGAN DYSFUNCTION SYNDROME12 reports
NEURALGIA12 reports
NIGHT SWEATS12 reports
PLEURAL EFFUSION12 reports
PRODUCT USE IN UNAPPROVED INDICATION12 reports
WOUND12 reports
BACTERIAL INFECTION11 reports
BLISTER11 reports
BURSITIS11 reports
CARDIAC ARREST11 reports
DRUG INTERACTION11 reports
DUODENAL ULCER PERFORATION11 reports
FACET JOINT SYNDROME11 reports
FOLLICULITIS11 reports
HAND DEFORMITY11 reports
HEPATIC ENZYME INCREASED11 reports
HYPOPHOSPHATAEMIA11 reports
IMPAIRED HEALING11 reports
INFLAMMATION11 reports
JOINT RANGE OF MOTION DECREASED11 reports
JOINT SWELLING11 reports
LIP DRY11 reports
LIVER INJURY11 reports
MALAISE11 reports
MUSCLE INJURY11 reports
NASOPHARYNGITIS11 reports
OBESITY11 reports
OSTEOARTHRITIS11 reports
PEMPHIGUS11 reports

Report Outcomes

Out of 284 classified reports for PANTHENOL:

Serious 93.7%Non-Serious 6.3%

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

Male132 (50.2%)
Female129 (49.0%)
Unknown2 (0.8%)

Reports by Age

Age 8034 reports
Age 4314 reports
Age 487 reports
Age 537 reports
Age 567 reports
Age 607 reports
Age 686 reports
Age 876 reports
Age 695 reports
Age 715 reports
Age 765 reports
Age 74 reports
Age 114 reports
Age 244 reports
Age 314 reports
Age 384 reports
Age 514 reports
Age 574 reports
Age 614 reports
Age 624 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 PANTHENOL?

This profile reflects 1,581 FDA FAERS reports that mention PANTHENOL. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for PANTHENOL?

Frequently reported terms in FAERS include NAUSEA, GENERAL PHYSICAL HEALTH DETERIORATION, CONDITION AGGRAVATED, DYSPNOEA, VOMITING, ABDOMINAL PAIN. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures PANTHENOL?

Labeling and FAERS entries often list LAON COMMERCE co ltd in connection with PANTHENOL. 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.