BRYONIA ALBA ROOT

N/A

Manufactured by Energique, Inc.

26 FDA adverse event reports analyzed

Last updated: 2026-04-15

About BRYONIA ALBA ROOT

BRYONIA ALBA ROOT is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Energique, Inc.. The most commonly reported adverse reactions for BRYONIA ALBA ROOT include ABNORMAL SENSATION IN EYE, ASTHMA, BALANCE DISORDER, BLOOD GLUCOSE DECREASED, CHEST DISCOMFORT. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for BRYONIA ALBA ROOT.

Top Adverse Reactions

ABNORMAL SENSATION IN EYE1 reports
ASTHMA1 reports
BALANCE DISORDER1 reports
BLOOD GLUCOSE DECREASED1 reports
CHEST DISCOMFORT1 reports
CHROMATURIA1 reports
DRUG INEFFECTIVE1 reports
DYSPNOEA1 reports
FAECES PALE1 reports
HEADACHE1 reports
HEPATITIS ACUTE1 reports
HOT FLUSH1 reports
HYPERHIDROSIS1 reports
HYPERTENSION1 reports
INFLUENZA1 reports
INSOMNIA1 reports
MEMORY IMPAIRMENT1 reports
MOOD SWINGS1 reports
MYALGIA1 reports
NAUSEA1 reports
OROPHARYNGEAL PAIN1 reports
PULMONARY CONGESTION1 reports
SENSATION OF HEAVINESS1 reports
SENSORY LOSS1 reports
SNEEZING1 reports
SYNCOPE1 reports

Report Outcomes

Out of 5 classified reports for BRYONIA ALBA ROOT:

Serious 60.0%Non-Serious 40.0%

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

Female4 (80.0%)
Male1 (20.0%)

Reports by Age

Age 301 reports
Age 611 reports
Age 761 reports
Age 771 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 BRYONIA ALBA ROOT?

This profile reflects 26 FDA FAERS reports that mention BRYONIA ALBA ROOT. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for BRYONIA ALBA ROOT?

Frequently reported terms in FAERS include ABNORMAL SENSATION IN EYE, ASTHMA, BALANCE DISORDER, BLOOD GLUCOSE DECREASED, CHEST DISCOMFORT, CHROMATURIA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures BRYONIA ALBA ROOT?

Labeling and FAERS entries often list Energique, Inc. in connection with BRYONIA ALBA 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.