GELSEMIUM SEMPERVIRENS ROOT

N/A

Manufactured by Boiron

39 FDA adverse event reports analyzed

Last updated: 2026-04-15

About GELSEMIUM SEMPERVIRENS ROOT

GELSEMIUM SEMPERVIRENS ROOT is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Boiron. The most commonly reported adverse reactions for GELSEMIUM SEMPERVIRENS ROOT include RASH, HEPATITIS, PANCREATITIS, INSOMNIA, ACNE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for GELSEMIUM SEMPERVIRENS ROOT.

Top Adverse Reactions

RASH6 reports
HEPATITIS4 reports
PANCREATITIS4 reports
INSOMNIA3 reports
ACNE2 reports
DRUG INTOLERANCE2 reports
HEADACHE2 reports
HYPOTENSION2 reports
MALAISE2 reports
MYOCARDIAL INFARCTION2 reports
SLEEP APNOEA SYNDROME2 reports
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS1 reports
ASTHENOPIA1 reports
DRY EYE1 reports
EYELID PTOSIS1 reports
ILL DEFINED DISORDER1 reports
MUSCULAR WEAKNESS1 reports
PARALYSIS1 reports
URINARY RETENTION1 reports

Report Outcomes

Out of 11 classified reports for GELSEMIUM SEMPERVIRENS ROOT:

Serious 90.9%Non-Serious 9.1%

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

Female9 (100.0%)

Reports by Age

Age 716 reports
Age 601 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 GELSEMIUM SEMPERVIRENS ROOT?

This profile reflects 39 FDA FAERS reports that mention GELSEMIUM SEMPERVIRENS ROOT. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for GELSEMIUM SEMPERVIRENS ROOT?

Frequently reported terms in FAERS include RASH, HEPATITIS, PANCREATITIS, INSOMNIA, ACNE, DRUG INTOLERANCE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures GELSEMIUM SEMPERVIRENS ROOT?

Labeling and FAERS entries often list Boiron in connection with GELSEMIUM SEMPERVIRENS ROOT. 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.