AVENA SATIVA FLOWERING TOP

N/A

168 FDA adverse event reports analyzed

Last updated: 2026-04-15

About AVENA SATIVA FLOWERING TOP

AVENA SATIVA FLOWERING TOP is a medication tracked in the FDA Adverse Event Reporting System (FAERS). The most commonly reported adverse reactions for AVENA SATIVA FLOWERING TOP include PRURITUS, LIVER FUNCTION TEST INCREASED, RASH, ACUTE CORONARY SYNDROME, ALANINE AMINOTRANSFERASE INCREASED. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for AVENA SATIVA FLOWERING TOP.

Top Adverse Reactions

PRURITUS7 reports
LIVER FUNCTION TEST INCREASED4 reports
RASH4 reports
ACUTE CORONARY SYNDROME3 reports
ALANINE AMINOTRANSFERASE INCREASED3 reports
BACK PAIN3 reports
BLOOD PRESSURE FLUCTUATION3 reports
CONSTIPATION3 reports
CREPITATIONS3 reports
DRY SKIN3 reports
HERPES ZOSTER3 reports
INFECTION3 reports
NAUSEA3 reports
PAIN IN EXTREMITY3 reports
SKIN HAEMORRHAGE3 reports
URTICARIA3 reports
ACNE2 reports
ARTHRALGIA2 reports
BLISTER2 reports
BLOOD ALKALINE PHOSPHATASE INCREASED2 reports
BLOOD LACTATE DEHYDROGENASE INCREASED2 reports
BREAST PAIN2 reports
BREAST TENDERNESS2 reports
CONTUSION2 reports
DERMATITIS CONTACT2 reports
DISCOMFORT2 reports
DYSGEUSIA2 reports
EPISTAXIS2 reports
ERYTHEMA2 reports
FATIGUE2 reports
GASTROOESOPHAGEAL REFLUX DISEASE2 reports
HAEMORRHAGE2 reports
HYPERSENSITIVITY2 reports
HYPOPHAGIA2 reports
MALAISE2 reports
MUCOSAL INFLAMMATION2 reports
NASOPHARYNGITIS2 reports
PAIN IN JAW2 reports
PIGMENTATION DISORDER2 reports
PNEUMONIA2 reports
POLLAKIURIA2 reports
SKIN BURNING SENSATION2 reports
SKIN CANCER2 reports
SKIN REACTION2 reports
THROMBOSIS IN DEVICE2 reports
TREMOR2 reports
ABASIA1 reports
ABDOMINAL PAIN UPPER1 reports
ACQUIRED OESOPHAGEAL WEB1 reports
ACUTE MYOCARDIAL INFARCTION1 reports
AMNESIA1 reports
ANAEMIA1 reports
ANTI THYROID ANTIBODY POSITIVE1 reports
ANXIETY1 reports
AORTIC ARTERIOSCLEROSIS1 reports
AORTIC CALCIFICATION1 reports
ARTERIOSCLEROSIS1 reports
ASTHENIA1 reports
ASTHMA1 reports
AUTONOMIC NEUROPATHY1 reports
BALANCE DISORDER1 reports
BLOOD CHOLESTEROL INCREASED1 reports
BLOOD CREATINE PHOSPHOKINASE INCREASED1 reports
BLOOD GLUCOSE INCREASED1 reports
BLOOD PHOSPHORUS INCREASED1 reports
BLOOD PRESSURE ABNORMAL1 reports
BLOOD PRESSURE INCREASED1 reports
BLOOD TESTOSTERONE ABNORMAL1 reports
BLOOD TRIGLYCERIDES INCREASED1 reports
BONE DENSITY DECREASED1 reports
BONE PAIN1 reports
BREAST HYPERPLASIA1 reports
BRONCHITIS1 reports
CARDIAC FAILURE CONGESTIVE1 reports
CARDIOMEGALY1 reports
CARDIOMYOPATHY1 reports
CAROTID ARTERY STENOSIS1 reports
CATARACT1 reports
CELLULITIS1 reports
CERUMEN IMPACTION1 reports
CHEST PAIN1 reports
CHOLELITHIASIS1 reports
COCCIDIOIDOMYCOSIS1 reports
COGNITIVE DISORDER1 reports
CORONARY ARTERY DISEASE1 reports
COUGH1 reports
DECREASED INTEREST1 reports
DEEP VEIN THROMBOSIS1 reports
DEFORMITY1 reports
DEMENTIA ALZHEIMER^S TYPE1 reports
DEMENTIA WITH LEWY BODIES1 reports
DERMATOPHYTOSIS1 reports
DIARRHOEA1 reports
DIASTOLIC DYSFUNCTION1 reports
DISTURBANCE IN ATTENTION1 reports
DIZZINESS1 reports
DRUG HYPERSENSITIVITY1 reports
DRUG INTERACTION1 reports
DRY EYE1 reports
DYSPHAGIA1 reports

Report Outcomes

Out of 24 classified reports for AVENA SATIVA FLOWERING TOP:

Serious 91.7%Non-Serious 8.3%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Frequently Asked Questions

How many FDA adverse event reports are associated with AVENA SATIVA FLOWERING TOP?

This profile reflects 168 FDA FAERS reports that mention AVENA SATIVA FLOWERING TOP. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for AVENA SATIVA FLOWERING TOP?

Frequently reported terms in FAERS include PRURITUS, LIVER FUNCTION TEST INCREASED, RASH, ACUTE CORONARY SYNDROME, ALANINE AMINOTRANSFERASE INCREASED, BACK PAIN. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

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.