BUFFERED ASPIRIN

N/A

Manufactured by Lil' Drug Store Products, Inc.

4,540 FDA adverse event reports analyzed

Last updated: 2026-04-14

About BUFFERED ASPIRIN

BUFFERED ASPIRIN is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Lil' Drug Store Products, Inc.. The most commonly reported adverse reactions for BUFFERED ASPIRIN include CHRONIC KIDNEY DISEASE, ACUTE KIDNEY INJURY, RENAL FAILURE, END STAGE RENAL DISEASE, RENAL INJURY. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for BUFFERED ASPIRIN.

Top Adverse Reactions

CHRONIC KIDNEY DISEASE721 reports
ACUTE KIDNEY INJURY439 reports
RENAL FAILURE395 reports
END STAGE RENAL DISEASE256 reports
RENAL INJURY179 reports
GASTROOESOPHAGEAL REFLUX DISEASE117 reports
NEPHROGENIC ANAEMIA117 reports
REBOUND ACID HYPERSECRETION78 reports
DEPRESSION72 reports
NAUSEA72 reports
OSTEOPOROSIS68 reports
TUBULOINTERSTITIAL NEPHRITIS64 reports
FATIGUE61 reports
DIARRHOEA56 reports
HEADACHE55 reports
HYPERPARATHYROIDISM SECONDARY54 reports
ANXIETY49 reports
DYSPNOEA49 reports
ARTHRITIS48 reports
DYSPEPSIA48 reports
MULTIPLE FRACTURES45 reports
PAIN45 reports
DRUG INEFFECTIVE42 reports
CONDITION AGGRAVATED38 reports
NEPHROPATHY35 reports
ABDOMINAL PAIN UPPER33 reports
MALAISE33 reports
DEATH32 reports
WEIGHT DECREASED32 reports
FALL31 reports
VOMITING31 reports
DIZZINESS30 reports
PNEUMONIA29 reports
COUGH28 reports
ARTHRALGIA26 reports
BONE DISORDER26 reports
CONSTIPATION26 reports
RENAL IMPAIRMENT26 reports
NASOPHARYNGITIS25 reports
OFF LABEL USE25 reports
ABDOMINAL PAIN24 reports
VITAMIN D DEFICIENCY24 reports
ASTHENIA23 reports
DIABETES MELLITUS23 reports
OSTEOARTHRITIS23 reports
PRODUCTIVE COUGH21 reports
CHRONIC KIDNEY DISEASE MINERAL AND BONE DISORDER20 reports
SOMNOLENCE20 reports
INSOMNIA19 reports
GAIT DISTURBANCE18 reports
HYPERTENSION18 reports
WHEEZING18 reports
BACK PAIN17 reports
CALCIUM DEFICIENCY17 reports
CHEST PAIN17 reports
INTERVERTEBRAL DISC DEGENERATION17 reports
ANAEMIA16 reports
ANKLE FRACTURE16 reports
ARTHROPATHY16 reports
CEREBROVASCULAR ACCIDENT16 reports
DECREASED APPETITE16 reports
PAIN IN EXTREMITY16 reports
PULMONARY EMBOLISM16 reports
RASH16 reports
THERAPEUTIC PRODUCT EFFECT INCOMPLETE16 reports
FEELING ABNORMAL15 reports
HYPOXIA15 reports
MYOCARDIAL INFARCTION15 reports
ASTHMA14 reports
MUSCLE SPASMS14 reports
PYREXIA14 reports
SWELLING14 reports
ABDOMINAL DISCOMFORT13 reports
CARDIAC FAILURE CONGESTIVE13 reports
CATARACT13 reports
DRUG HYPERSENSITIVITY13 reports
ERYTHEMA13 reports
FOOT FRACTURE13 reports
INFLUENZA13 reports
INTERVERTEBRAL DISC PROTRUSION13 reports
PRODUCT DOSE OMISSION ISSUE13 reports
RENAL DISORDER13 reports
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION13 reports
ANGINA PECTORIS12 reports
ARTERIOSCLEROSIS12 reports
ARTERIOSCLEROSIS CORONARY ARTERY12 reports
CARPAL TUNNEL SYNDROME12 reports
FULL BLOOD COUNT ABNORMAL12 reports
LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES12 reports
MYCOTIC ALLERGY12 reports
NEPHROLITHIASIS12 reports
SEPSIS12 reports
THROMBOSIS12 reports
CARDIAC DISORDER11 reports
CONJUNCTIVITIS ALLERGIC11 reports
DEHYDRATION11 reports
DUST ALLERGY11 reports
GLAUCOMA11 reports
HYPERSENSITIVITY11 reports
HYPOTENSION11 reports

Report Outcomes

Out of 1,394 classified reports for BUFFERED ASPIRIN:

Serious 81.8%Non-Serious 18.2%

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

Female716 (56.5%)
Male550 (43.4%)
Unknown2 (0.2%)

Reports by Age

Age 7228 reports
Age 6026 reports
Age 6626 reports
Age 5825 reports
Age 6425 reports
Age 5424 reports
Age 6724 reports
Age 5322 reports
Age 5522 reports
Age 5622 reports
Age 5722 reports
Age 6321 reports
Age 6821 reports
Age 5920 reports
Age 6219 reports
Age 6519 reports
Age 6919 reports
Age 7119 reports
Age 7319 reports
Age 5018 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 BUFFERED ASPIRIN?

This profile reflects 4,540 FDA FAERS reports that mention BUFFERED ASPIRIN. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for BUFFERED ASPIRIN?

Frequently reported terms in FAERS include CHRONIC KIDNEY DISEASE, ACUTE KIDNEY INJURY, RENAL FAILURE, END STAGE RENAL DISEASE, RENAL INJURY, GASTROOESOPHAGEAL REFLUX DISEASE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures BUFFERED ASPIRIN?

Labeling and FAERS entries often list Lil' Drug Store Products, Inc. in connection with BUFFERED ASPIRIN. 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.