Product name as reported
Aspirin Cardio: adverse event reports filed with FDA
517 reports list it as a suspect or interacting product, 2004–2021.
- 517
- reports as suspect product
- 0% of all reports · about 23 a year
- 0
- reports, 12 months to June 2026
- 0 in the 12 months before
- 100%
- marked serious by the reporter
- 57.4% across all reports
- 15.5%
- record death among outcomes, as reported
- 80 reports · not verified by FDA
517 adverse event reports received by FDA list the product name "Aspirin Cardio" as reporters wrote it as a suspect or interacting product, from February 2004 to August 2021. A further 1,422 reports list it only as a concomitant medication, and those are not counted in the figures on this page.
In the 12 months to June 2026, 0 reports listed it, and none in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Over its reporting history that is about 23 reports a year and 0% of the 20,646,523 reports in the database. How many people take it is not in the data, so a count is not a rate of occurrence.
Reporters most often recorded drug interaction (16.8%), gastrointestinal haemorrhage (11%) and haemorrhagic anaemia (11%). A report can list several reactions, so shares add to more than 100%; 223 different terms appear across these reports. Drug interaction is recorded in 16.8% of these reports, against 0.8% of all reports in the database.
100% of the reports are marked serious by the reporter; 15.5% record death among the outcomes and 70.2% record hospitalisation, as reported. 49.7% of the reports came from physicians, and the largest patient age group is 75 and over (48%). FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event."
Reports by month, five years
Reports by the month FDA received them. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases.
By year received
Reactions recorded in the reports
share of Aspirin Cardio reports recording the termall reports in the database
- Drug interactionan interaction between medicines16.8%87
- Gastrointestinal haemorrhagebleeding in the stomach or bowel11%57
- Haemorrhagic anaemia11%57
- Anaemialow red blood cells10.1%52
- Melaenablack tarry stools8.3%43
- Cerebral haemorrhage7.4%38
- Acute kidney injurysudden loss of kidney function5.8%30
- Falla fall4.8%25
- Hypotensionlow blood pressure4.8%25
- Thrombocytopenialow platelets3.5%18
- International normalised ratio increasedblood clotting slower than intended (raised INR)3.3%17
- Cerebrovascular accidentstroke2.9%15
- Epistaxisnosebleed2.9%15
- Haematuriablood in the urine2.9%15
- Haemorrhagebleeding2.9%15
- Astheniaweakness or lack of energy2.7%14
- Gastric ulcera stomach ulcer2.7%14
- Leukopenialow white blood cells2.7%14
- Syncopefainting2.7%14
- Haematomaa collection of blood under the skin or in tissue2.1%11
- Haematemesis1.9%10
- Pancytopenialow counts of all blood cells1.9%10
- Angina pectoris1.7%9
- Blood pressure decreaseda low blood pressure reading1.7%9
- Dyspnoeashortness of breath1.7%9
- Haemoglobin decreasedlow haemoglobin1.7%9
- Hemiparesis1.7%9
Top 30 of 223 MedDRA preferred terms recorded across these reports, with a plain-language gloss where one is available. One report can record several terms. The hollow bar is the share of all reports in the database; it describes the reports, not the patients. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."
Outcomes recorded
Outcome flags as the reporter set them; a report can carry several, and "other serious" is FDA's own category for serious reports outside the named outcomes. Grey bar: all 20,646,523 reports. FDA has not verified any outcome and states that the reports "cannot be used to estimate the incidence of these events."
Patients and reporters
Patient age
Patient sex
Who reported
Age and sex as stated in the report; the reporter's qualification is the primary source recorded by FDA. 1.4% of reports give the United States as the country of the event or reporter.
Reason for use recorded
| Indication as recorded (MedDRA) | Reports | Share |
|---|---|---|
| Coronary artery disease | 48 | 9.3% |
| Acute myocardial infarction | 11 | 2.1% |
| Myocardial ischaemia | 11 | 2.1% |
| Anticoagulant therapy | 6 | 1.2% |
| Cardiac disorder | 6 | 1.2% |
| Coronary artery bypass | 6 | 1.2% |
The indication field is filled in by the reporter and is often blank; shares are of all 517 reports.
In context
| Measure | Aspirin Cardio | All reports |
|---|---|---|
| Reports as suspect product | 517 | 20,646,523 |
| Share of that pool | — | 0% |
| Reports, latest 12 months | 0 | 1,332,454 |
| Marked serious | 100% | 57.4% |
| Death recorded among outcomes, per 1,000 reports | 155 | 91 |
| Hospitalisation recorded, per 1,000 reports | 702 | 213 |
| Consumer-filed share | 11.8% | 45.8% |
| Top term, share of reports | Drug interaction 16.8% | 0.8% |
Shares are of reports, not of patients treated. The number of people taking a product is not in the data, so none of these figures is a rate, and differences between columns reflect who takes a product, who reports and how long it has been sold. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."
Questions about Aspirin Cardio reports
How many adverse event reports has FDA received for Aspirin Cardio?
517 reports list Aspirin Cardio as a suspect or interacting product in the openFDA FAERS release of 28 Sep 2026, covering reports received through June 2026. 0 of them arrived in the latest 12 months. Another 1,422 list it only as a concomitant medication.
What reactions are recorded in Aspirin Cardio reports?
drug interaction (16.8%), gastrointestinal haemorrhage (11%), haemorrhagic anaemia (11%), anaemia (10.1%) and melaena (8.3%). These are MedDRA preferred terms coded from what the reporter described; a report can list several, and a term's presence is not a finding that Aspirin Cardio was responsible.
How serious are the reports?
100% are marked serious by the reporter. Among the outcomes recorded, 15.5% of reports include death and 70.2% include hospitalisation. FDA has not verified these outcomes and states that the reports "cannot be used to estimate the incidence" of the events.
Who files these reports?
physician (49.7%), other health professional (31.1%) and consumer or non-health professional (11.8%). Most reports reach FDA through the manufacturer, which must forward reports it receives.
Are reports for Aspirin Cardio rising?
0 reports in the 12 months to June 2026, and none in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Counts also move with how many people take a product, its time on the market and publicity.
Do these reports show that Aspirin Cardio was responsible for these reactions?
No. FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event." The reaction may relate to the condition being treated, to other medicines, or to something else.
Is this a list of the side effects of Aspirin Cardio?
No. It is a count of what was reported to FDA. The adverse reactions observed in clinical studies are printed on the FDA-approved label, which a pharmacist or clinician can go through with you.
How do I report an adverse event?
Consumers and health professionals can report to FDA through MedWatch (Form FDA 3500 online, or 1-800-FDA-1088), or to the manufacturer, which must pass reports on. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Drug Adverse Event (FAERS) bulk export released 28 Sep 2026, which holds reports FDA received through 30 Jun 2026. Drug names are as reported, resolved to the brand or generic name on the FDA label where openFDA's harmonisation matched them; classes are the pharmacologic class (EPC) from the label and the National Drug Code Directory of 17 Sep 2026. A report counts here when it lists Aspirin Cardio as a suspect or interacting product; reports listing it only as a concomitant medication (1,422) are excluded. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.