ASPIRIN LOW DOSE

N/A

Manufactured by AARNA USA INC.

2,041 FDA adverse event reports analyzed

Last updated: 2026-04-14

About ASPIRIN LOW DOSE

ASPIRIN LOW DOSE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by AARNA USA INC.. The most commonly reported adverse reactions for ASPIRIN LOW DOSE include DIARRHOEA, FATIGUE, PNEUMONIA, NAUSEA, DEATH. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ASPIRIN LOW DOSE.

Top Adverse Reactions

DIARRHOEA89 reports
FATIGUE86 reports
PNEUMONIA61 reports
NAUSEA58 reports
DEATH51 reports
ASTHENIA50 reports
DYSPNOEA47 reports
DRUG INEFFECTIVE43 reports
VOMITING41 reports
RASH39 reports
DECREASED APPETITE38 reports
DIZZINESS38 reports
HEADACHE34 reports
MALAISE33 reports
FALL32 reports
PAIN29 reports
WEIGHT DECREASED29 reports
WHITE BLOOD CELL COUNT DECREASED29 reports
BACK PAIN27 reports
COUGH26 reports
PERIPHERAL SWELLING26 reports
CONSTIPATION25 reports
URINARY TRACT INFECTION25 reports
DISEASE PROGRESSION23 reports
DRUG DOSE OMISSION23 reports
PRURITUS23 reports
PYREXIA23 reports
GAIT DISTURBANCE22 reports
MYOCARDIAL INFARCTION22 reports
NEUROPATHY PERIPHERAL22 reports
PLASMA CELL MYELOMA22 reports
ABDOMINAL PAIN UPPER21 reports
MUSCLE SPASMS21 reports
PAIN IN EXTREMITY21 reports
PLATELET COUNT DECREASED21 reports
FLUSHING20 reports
FULL BLOOD COUNT DECREASED20 reports
INSOMNIA20 reports
ABDOMINAL DISCOMFORT19 reports
ABDOMINAL PAIN18 reports
CHEST PAIN18 reports
HYPOAESTHESIA18 reports
OFF LABEL USE18 reports
ANAEMIA17 reports
MEMORY IMPAIRMENT17 reports
PRODUCT DOSE OMISSION17 reports
TREMOR17 reports
ALOPECIA15 reports
DEHYDRATION15 reports
MUSCULAR WEAKNESS15 reports
UNEVALUABLE EVENT15 reports
DEPRESSION14 reports
MULTIPLE SCLEROSIS RELAPSE14 reports
MYALGIA14 reports
NASOPHARYNGITIS14 reports
OEDEMA PERIPHERAL14 reports
ARTHRALGIA13 reports
CATARACT13 reports
CHRONIC OBSTRUCTIVE PULMONARY DISEASE13 reports
HAEMOGLOBIN DECREASED13 reports
HYPERTENSION13 reports
HYPOTENSION13 reports
INFECTION13 reports
LABORATORY TEST ABNORMAL13 reports
THROMBOSIS13 reports
ABDOMINAL DISTENSION12 reports
BLOOD GLUCOSE INCREASED12 reports
FEELING ABNORMAL12 reports
WEIGHT INCREASED12 reports
ADVERSE DRUG REACTION11 reports
CARDIAC DISORDER11 reports
CARDIAC FAILURE CONGESTIVE11 reports
CONTUSION11 reports
EPISTAXIS11 reports
GASTROINTESTINAL DISORDER11 reports
GASTROOESOPHAGEAL REFLUX DISEASE11 reports
HEART RATE INCREASED11 reports
HOSPITALISATION11 reports
HOT FLUSH11 reports
INFLUENZA11 reports
SKIN DISCOLOURATION11 reports
BALANCE DISORDER10 reports
CONDITION AGGRAVATED10 reports
DYSPEPSIA10 reports
DYSPHONIA10 reports
HYPERHIDROSIS10 reports
PARAESTHESIA10 reports
BLOOD COUNT ABNORMAL9 reports
CEREBROVASCULAR ACCIDENT9 reports
ERYTHEMA9 reports
HAEMORRHAGE9 reports
JOINT SWELLING9 reports
LOSS OF CONSCIOUSNESS9 reports
MUSCULOSKELETAL DISORDER9 reports
NEUTROPENIA9 reports
SEPSIS9 reports
SINUSITIS9 reports
SOMNOLENCE9 reports
ADVERSE EVENT8 reports
ANXIETY8 reports

Report Outcomes

Out of 1,197 classified reports for ASPIRIN LOW DOSE:

Serious 60.3%Non-Serious 39.7%

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

Female660 (56.0%)
Male518 (44.0%)

Reports by Age

Age 7632 reports
Age 6531 reports
Age 6631 reports
Age 7430 reports
Age 6928 reports
Age 7525 reports
Age 7223 reports
Age 7122 reports
Age 7822 reports
Age 5921 reports
Age 6721 reports
Age 7021 reports
Age 7921 reports
Age 6420 reports
Age 7320 reports
Age 6319 reports
Age 7719 reports
Age 8019 reports
Age 5818 reports
Age 6018 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 LOW DOSE?

This profile reflects 2,041 FDA FAERS reports that mention ASPIRIN LOW DOSE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for ASPIRIN LOW DOSE?

Frequently reported terms in FAERS include DIARRHOEA, FATIGUE, PNEUMONIA, NAUSEA, DEATH, ASTHENIA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures ASPIRIN LOW DOSE?

Labeling and FAERS entries often list AARNA USA INC. in connection with ASPIRIN LOW DOSE. 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.