ASPIRIN, CAFFEINE

N/A

Manufactured by CVS Pharmacy

45 FDA adverse event reports analyzed

Last updated: 2026-04-15

About ASPIRIN, CAFFEINE

ASPIRIN, CAFFEINE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by CVS Pharmacy. The most commonly reported adverse reactions for ASPIRIN, CAFFEINE include RASH, THERAPEUTIC RESPONSE UNEXPECTED, AMNESIA, ANAPHYLACTOID REACTION, ATAXIA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ASPIRIN, CAFFEINE.

Top Adverse Reactions

RASH3 reports
THERAPEUTIC RESPONSE UNEXPECTED2 reports
AMNESIA1 reports
ANAPHYLACTOID REACTION1 reports
ATAXIA1 reports
ATRIAL FIBRILLATION1 reports
BALANCE DISORDER1 reports
BLOOD PRESSURE INCREASED1 reports
CEREBELLAR ATROPHY1 reports
CONSTIPATION1 reports
COORDINATION ABNORMAL1 reports
DIZZINESS1 reports
DRUG ERUPTION1 reports
DRUG INEFFECTIVE1 reports
DYSPHAGIA1 reports
GAIT DISTURBANCE1 reports
HALLUCINATION1 reports
HEADACHE1 reports
HEART RATE INCREASED1 reports
IMPAIRED DRIVING ABILITY1 reports
INFECTION1 reports
INJECTION SITE ERYTHEMA1 reports
INJECTION SITE PRURITUS1 reports
INJECTION SITE RASH1 reports
INJECTION SITE SWELLING1 reports
LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES1 reports
MUSCULAR WEAKNESS1 reports
NEUROPATHY PERIPHERAL1 reports
OFF LABEL USE1 reports
PAIN1 reports
PRODUCT FORMULATION ISSUE1 reports
PRODUCT SUBSTITUTION ISSUE1 reports
PRODUCT USE ISSUE1 reports
PRURITUS1 reports
RASH PAPULAR1 reports
RASH PRURITIC1 reports
SOMNOLENCE1 reports
SPEECH DISORDER1 reports
THERAPEUTIC PRODUCT EFFECT INCOMPLETE1 reports
TREMOR1 reports
VISION BLURRED1 reports
VOMITING1 reports

Report Outcomes

Out of 8 classified reports for ASPIRIN, CAFFEINE:

Serious 62.5%Non-Serious 37.5%

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

Female7 (87.5%)
Male1 (12.5%)

Reports by Age

Age 411 reports
Age 451 reports
Age 461 reports
Age 511 reports
Age 521 reports
Age 681 reports
Age 831 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, CAFFEINE?

This profile reflects 45 FDA FAERS reports that mention ASPIRIN, CAFFEINE. Reporting is voluntary and does not prove that the drug caused any listed event.

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

Frequently reported terms in FAERS include RASH, THERAPEUTIC RESPONSE UNEXPECTED, AMNESIA, ANAPHYLACTOID REACTION, ATAXIA, ATRIAL FIBRILLATION. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures ASPIRIN, CAFFEINE?

Labeling and FAERS entries often list CVS Pharmacy in connection with ASPIRIN, 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.