ATROPA BELLADONNA

N/A

489 FDA adverse event reports analyzed

Last updated: 2026-04-15

About ATROPA BELLADONNA

ATROPA BELLADONNA is a medication tracked in the FDA Adverse Event Reporting System (FAERS). The most commonly reported adverse reactions for ATROPA BELLADONNA include DIARRHOEA, NAUSEA, CHEST PAIN, ASTHENIA, PAIN. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ATROPA BELLADONNA.

Top Adverse Reactions

DIARRHOEA22 reports
NAUSEA21 reports
CHEST PAIN12 reports
ASTHENIA11 reports
PAIN11 reports
DRUG INEFFECTIVE10 reports
INSOMNIA10 reports
VOMITING10 reports
ALOPECIA9 reports
BACK PAIN9 reports
DYSPNOEA9 reports
ARTHRALGIA8 reports
DECREASED APPETITE8 reports
HEADACHE8 reports
ABDOMINAL PAIN7 reports
ABDOMINAL PAIN UPPER7 reports
CORONARY ARTERY DISEASE7 reports
DEHYDRATION7 reports
MYOCARDIAL INFARCTION7 reports
PNEUMONIA7 reports
URINARY TRACT INFECTION7 reports
DRUG HYPERSENSITIVITY6 reports
DYSPEPSIA6 reports
GASTROOESOPHAGEAL REFLUX DISEASE6 reports
HYPERTENSION6 reports
MALAISE6 reports
OFF LABEL USE6 reports
WEIGHT DECREASED6 reports
ABDOMINAL DISTENSION5 reports
ANXIETY5 reports
CHEST DISCOMFORT5 reports
CROHN'S DISEASE5 reports
DEPRESSION5 reports
DRUG DOSE OMISSION5 reports
FATIGUE5 reports
HYPERHIDROSIS5 reports
HYPOPHOSPHATAEMIA5 reports
MENTAL DISORDER5 reports
PAIN IN EXTREMITY5 reports
ACUTE KIDNEY INJURY4 reports
AGRANULOCYTOSIS4 reports
CHRONIC KIDNEY DISEASE4 reports
DEATH4 reports
DIABETES MELLITUS4 reports
EMOTIONAL DISTRESS4 reports
FALL4 reports
FOCAL SEGMENTAL GLOMERULOSCLEROSIS4 reports
MIGRAINE4 reports
NASOPHARYNGITIS4 reports
RASH4 reports
RENAL FAILURE4 reports
SOMNOLENCE4 reports
WEIGHT INCREASED4 reports
WRONG TECHNIQUE IN DRUG USAGE PROCESS4 reports
ABDOMINAL DISCOMFORT3 reports
AMNESIA3 reports
ANAEMIA3 reports
ANGINA PECTORIS3 reports
ASTHMA3 reports
DISEASE PROGRESSION3 reports
EOSINOPHILIA3 reports
FEELING ABNORMAL3 reports
GASTRIC DISORDER3 reports
HERPES ZOSTER3 reports
HOT FLUSH3 reports
HYPERLIPIDAEMIA3 reports
HYPOKALAEMIA3 reports
HYPOTENSION3 reports
HYPOTHYROIDISM3 reports
INFLUENZA3 reports
INJECTION SITE PAIN3 reports
INJURY3 reports
IRRITABLE BOWEL SYNDROME3 reports
JAUNDICE3 reports
LETHARGY3 reports
MUSCLE SPASMS3 reports
OEDEMA PERIPHERAL3 reports
PARAESTHESIA3 reports
PRODUCT QUALITY ISSUE3 reports
PROTEINURIA3 reports
PRURITUS3 reports
PYREXIA3 reports
RASH ERYTHEMATOUS3 reports
SINUSITIS3 reports
TYPE 2 DIABETES MELLITUS3 reports
URTICARIA3 reports
VISION BLURRED3 reports
ACUTE MYOCARDIAL INFARCTION2 reports
ADVERSE EVENT2 reports
AGITATION2 reports
ARTERIOSCLEROSIS CORONARY ARTERY2 reports
ARTHRITIS2 reports
BALANCE DISORDER2 reports
BLOOD GLUCOSE DECREASED2 reports
BLOOD GLUCOSE INCREASED2 reports
BLOOD MAGNESIUM DECREASED2 reports
BLOOD POTASSIUM DECREASED2 reports
BLOOD PRESSURE DECREASED2 reports
BRADYCARDIA2 reports
BRONCHITIS2 reports

Demographics Breakdown

Reports by Age

Age 478 reports
Age 436 reports
Age 526 reports
Age 555 reports
Age 605 reports
Age 615 reports
Age 745 reports
Age 314 reports
Age 534 reports
Age 654 reports
Age 784 reports
Age 383 reports
Age 623 reports
Age 673 reports
Age 92 reports
Age 302 reports
Age 482 reports
Age 592 reports
Age 632 reports
Age 642 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 ATROPA BELLADONNA?

This profile reflects 489 FDA FAERS reports that mention ATROPA BELLADONNA. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for ATROPA BELLADONNA?

Frequently reported terms in FAERS include DIARRHOEA, NAUSEA, CHEST PAIN, ASTHENIA, PAIN, DRUG INEFFECTIVE. 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.