ASPIRIN AND CAFFEINE

N/A

Manufactured by Medtech Products Inc.

684 FDA adverse event reports analyzed

Last updated: 2026-04-15

About ASPIRIN AND CAFFEINE

ASPIRIN AND CAFFEINE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Medtech Products Inc.. The most commonly reported adverse reactions for ASPIRIN AND CAFFEINE include DRUG INEFFECTIVE, HEADACHE, NAUSEA, PAIN, ARTHRALGIA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ASPIRIN AND CAFFEINE.

Top Adverse Reactions

DRUG INEFFECTIVE33 reports
HEADACHE28 reports
NAUSEA24 reports
PAIN23 reports
ARTHRALGIA15 reports
DYSPNOEA15 reports
FATIGUE14 reports
FEELING ABNORMAL14 reports
VOMITING14 reports
BACK PAIN13 reports
INJECTION SITE PAIN12 reports
ANAEMIA11 reports
MALAISE11 reports
FALL10 reports
ABDOMINAL PAIN9 reports
CHEST PAIN9 reports
DIARRHOEA9 reports
PAIN IN EXTREMITY9 reports
ANXIETY8 reports
CHRONIC KIDNEY DISEASE8 reports
DEPRESSION8 reports
DRUG HYPERSENSITIVITY8 reports
GASTRIC ULCER8 reports
GASTROINTESTINAL HAEMORRHAGE8 reports
LOSS OF CONSCIOUSNESS8 reports
MIGRAINE8 reports
OFF LABEL USE8 reports
UPPER GASTROINTESTINAL HAEMORRHAGE8 reports
WEIGHT INCREASED8 reports
ABDOMINAL PAIN UPPER7 reports
ASTHENIA7 reports
DEPENDENCE7 reports
DRUG DEPENDENCE7 reports
HYPERTENSION7 reports
INCORRECT DOSE ADMINISTERED7 reports
OVERDOSE7 reports
PRURITUS7 reports
RASH7 reports
TOXICITY TO VARIOUS AGENTS7 reports
CEREBROVASCULAR ACCIDENT6 reports
COUGH6 reports
DIZZINESS6 reports
GAIT DISTURBANCE6 reports
PNEUMONIA6 reports
RENAL FAILURE6 reports
ULCER6 reports
WEIGHT DECREASED6 reports
ABDOMINAL DISCOMFORT5 reports
ACUTE KIDNEY INJURY5 reports
ANHEDONIA5 reports
CONSTIPATION5 reports
DECREASED APPETITE5 reports
EMOTIONAL DISTRESS5 reports
GASTRIC HAEMORRHAGE5 reports
HAEMORRHAGE5 reports
INJECTION SITE ERYTHEMA5 reports
MEMORY IMPAIRMENT5 reports
NASOPHARYNGITIS5 reports
PRODUCT QUALITY ISSUE5 reports
TACHYCARDIA5 reports
THERAPEUTIC RESPONSE UNEXPECTED5 reports
ACCIDENTAL OVERDOSE4 reports
BALANCE DISORDER4 reports
BLOOD PRESSURE INCREASED4 reports
CHEST DISCOMFORT4 reports
COLITIS4 reports
DYSPHAGIA4 reports
HOSPITALISATION4 reports
HYPOACUSIS4 reports
INCORRECT DRUG ADMINISTRATION DURATION4 reports
INCORRECT PRODUCT ADMINISTRATION DURATION4 reports
INJURY4 reports
INSOMNIA4 reports
MUSCLE SPASMS4 reports
PULMONARY EMBOLISM4 reports
RECTAL HAEMORRHAGE4 reports
ROAD TRAFFIC ACCIDENT4 reports
ULCER HAEMORRHAGE4 reports
URINARY TRACT INFECTION4 reports
ALOPECIA3 reports
AMNESIA3 reports
ANGER3 reports
ANKLE FRACTURE3 reports
BLOOD CHOLESTEROL INCREASED3 reports
BODY HEIGHT DECREASED3 reports
CARDIAC DISORDER3 reports
COAGULOPATHY3 reports
COVID 193 reports
DEATH3 reports
DEVICE ISSUE3 reports
DRUG ABUSE3 reports
DRUG EFFECT INCOMPLETE3 reports
DYSPHONIA3 reports
END STAGE RENAL DISEASE3 reports
ERYTHEMA3 reports
EYE DISORDER3 reports
FEAR3 reports
GENERAL PHYSICAL HEALTH DETERIORATION3 reports
HAEMATEMESIS3 reports
HAEMATOCHEZIA3 reports

Report Outcomes

Out of 296 classified reports for ASPIRIN AND CAFFEINE:

Serious 61.1%Non-Serious 38.9%

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

Female195 (70.7%)
Male75 (27.2%)
Unknown6 (2.2%)

Reports by Age

Age 4910 reports
Age 588 reports
Age 407 reports
Age 477 reports
Age 517 reports
Age 537 reports
Age 647 reports
Age 466 reports
Age 596 reports
Age 626 reports
Age 555 reports
Age 294 reports
Age 384 reports
Age 394 reports
Age 434 reports
Age 524 reports
Age 604 reports
Age 734 reports
Age 253 reports
Age 303 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 AND CAFFEINE?

This profile reflects 684 FDA FAERS reports that mention ASPIRIN AND CAFFEINE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for ASPIRIN AND CAFFEINE?

Frequently reported terms in FAERS include DRUG INEFFECTIVE, HEADACHE, NAUSEA, PAIN, ARTHRALGIA, DYSPNOEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures ASPIRIN AND CAFFEINE?

Labeling and FAERS entries often list Medtech Products Inc. in connection with ASPIRIN AND CAFFEINE. 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.