ASPIRIN 81MG

N/A

Manufactured by Allegiant Health

1,051 FDA adverse event reports analyzed

Last updated: 2026-04-14

About ASPIRIN 81MG

ASPIRIN 81MG is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Allegiant Health. The most commonly reported adverse reactions for ASPIRIN 81MG include DEATH, FATIGUE, NAUSEA, ANAEMIA, DISEASE PROGRESSION. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ASPIRIN 81MG.

Top Adverse Reactions

DEATH39 reports
FATIGUE32 reports
NAUSEA30 reports
ANAEMIA27 reports
DISEASE PROGRESSION27 reports
HEADACHE26 reports
VOMITING25 reports
DIARRHOEA22 reports
DYSPNOEA21 reports
FALL21 reports
DIZZINESS20 reports
HAEMORRHAGE20 reports
PAIN IN EXTREMITY20 reports
ASTHENIA19 reports
PRODUCT SUBSTITUTION ISSUE19 reports
DRUG INEFFECTIVE17 reports
GASTROINTESTINAL HAEMORRHAGE16 reports
PAIN16 reports
PERIPHERAL SWELLING16 reports
ABDOMINAL PAIN UPPER15 reports
ARTHRALGIA14 reports
PRURITUS14 reports
RASH13 reports
THERAPY INTERRUPTED13 reports
DECREASED APPETITE12 reports
ABDOMINAL DISCOMFORT11 reports
ANXIETY11 reports
HOSPITALISATION11 reports
HYPERTENSION11 reports
MYOCARDIAL INFARCTION11 reports
THERAPY CESSATION11 reports
APHASIA10 reports
BACK PAIN10 reports
BLOOD PRESSURE INCREASED10 reports
CEREBROVASCULAR ACCIDENT10 reports
CHEST PAIN10 reports
CONSTIPATION10 reports
MUSCLE SPASMS10 reports
URTICARIA10 reports
ALOPECIA9 reports
CONDITION AGGRAVATED9 reports
DEPRESSION9 reports
HOSPICE CARE9 reports
HYPOTENSION9 reports
INSOMNIA9 reports
VISUAL IMPAIRMENT9 reports
AMNESIA8 reports
COUGH8 reports
FEELING ABNORMAL8 reports
HYPERSENSITIVITY8 reports
MUSCULAR WEAKNESS8 reports
MYALGIA8 reports
PARAESTHESIA8 reports
PNEUMONIA8 reports
PYREXIA8 reports
RENAL FAILURE8 reports
URINARY TRACT INFECTION8 reports
ABDOMINAL PAIN7 reports
BLOOD GLUCOSE INCREASED7 reports
CHILLS7 reports
DEHYDRATION7 reports
DRUG HYPERSENSITIVITY7 reports
HAEMATOCHEZIA7 reports
HAEMOGLOBIN DECREASED7 reports
HYPOAESTHESIA7 reports
OEDEMA PERIPHERAL7 reports
SUBDURAL HAEMATOMA7 reports
TREMOR7 reports
BALANCE DISORDER6 reports
CEREBRAL HAEMORRHAGE6 reports
COVID 196 reports
DIABETIC KETOACIDOSIS6 reports
LABELLED DRUG DRUG INTERACTION MEDICATION ERROR6 reports
VISION BLURRED6 reports
WEIGHT DECREASED6 reports
AGITATION5 reports
ATRIAL FIBRILLATION5 reports
CARDIAC ARREST5 reports
CONFUSIONAL STATE5 reports
DYSPEPSIA5 reports
DYSPHAGIA5 reports
EYE PAIN5 reports
FLUID RETENTION5 reports
GAIT DISTURBANCE5 reports
HEART RATE IRREGULAR5 reports
HYPERHIDROSIS5 reports
INFUSION RELATED REACTION5 reports
LOSS OF CONSCIOUSNESS5 reports
MELAENA5 reports
NEUROPATHY PERIPHERAL5 reports
RECTAL HAEMORRHAGE5 reports
SWELLING5 reports
THROMBOSIS5 reports
UNRESPONSIVE TO STIMULI5 reports
VERTIGO5 reports
WEIGHT INCREASED5 reports
ASPARTATE AMINOTRANSFERASE INCREASED4 reports
BLISTER4 reports
BODY TEMPERATURE INCREASED4 reports
CHEST DISCOMFORT4 reports

Report Outcomes

Out of 684 classified reports for ASPIRIN 81MG:

Serious 72.5%Non-Serious 27.5%

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

Male342 (50.9%)
Female330 (49.1%)

Reports by Age

Age 7527 reports
Age 6926 reports
Age 6724 reports
Age 7223 reports
Age 7423 reports
Age 6822 reports
Age 7322 reports
Age 8021 reports
Age 6520 reports
Age 6620 reports
Age 8120 reports
Age 6218 reports
Age 6417 reports
Age 7017 reports
Age 7117 reports
Age 7617 reports
Age 6316 reports
Age 7716 reports
Age 6115 reports
Age 8715 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 ASPIRIN 81MG?

This profile reflects 1,051 FDA FAERS reports that mention ASPIRIN 81MG. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for ASPIRIN 81MG?

Frequently reported terms in FAERS include DEATH, FATIGUE, NAUSEA, ANAEMIA, DISEASE PROGRESSION, HEADACHE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures ASPIRIN 81MG?

Labeling and FAERS entries often list Allegiant Health in connection with ASPIRIN 81MG. 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.