Prescription medication · Direct Oral Anticoagulant (Factor Xa Inhibitor)

apixaban

Also sold as Eliquis. Apixaban is used to lower the chance of stroke in people with an irregular heartbeat called atrial fibrillation.

Data updated 2026-05-15

62,650
FDA reportsOften reported
12
InteractionsSeveral interactions
$9.51
Brand price (NADAC)

What the data shows

apixaban (Eliquis) is a prescription Direct Oral Anticoagulant (Factor Xa Inhibitor), more reported than most tracked drugs (62,650 FDA reports), with 12 documented drug interactions.

Reporting volume reflects how widely a drug is used and studied, not how dangerous it is, a FAERS report documents a temporal association, never proof of cause.

apixaban (Eliquis) is a prescription Direct Oral Anticoagulant (Factor Xa Inhibitor). Apixaban is used to lower the chance of stroke in people with an irregular heartbeat called atrial fibrillation.

Apixaban (Eliquis) is a medicine that helps prevent blood clots. It is used to lower the risk of stroke and other serious problems caused by blood clots.

Drug Pricing (NADAC)

Brand Price

$9.51/unit

Generic Available

Yes (3 manufacturers)

Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →

View Alternatives → Compare with Another Drug → Full Side Effects Report →

What it does

Apixaban is used to lower the chance of stroke in people with an irregular heartbeat called atrial fibrillation.

Common side effects

Bleeding more easily (like nosebleeds or heavier periods), Bruising more easily

Key warnings

Apixaban has two important warnings.

The sections below are summarized in plain English from apixaban's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.

How It Works

Apixaban is a type of drug called a factor Xa inhibitor. It works by blocking a substance in the blood that helps clots form. This helps to keep your blood flowing smoothly.

Side Effects (from patient reports)

Based on 62,650 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for apixaban, by number of reports

reports

What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.

Source FDA Adverse Event Reporting System (FAERS) As of 2025

Reports over time

Adverse-event reports filed for apixaban each year to the FDA Adverse Event Reporting System (FAERS).

05,00010,00015,00020,000 20052009201220152018202120242025 5,788

Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.

Where apixaban sits

apixaban has more FDA adverse-event reports than 77% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.

fewest reports most reports

Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is apixaban; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 62,650 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2005–2025.

Total Reports

62,650

Reports Mentioning Death

6,759

10.8% of reports — not proof of cause

Hospitalization Reports

27,509

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 27,064 (47%)
Male 30,594 (53%)

Age Distribution

0–17 457
18–44 1,817
45–64 8,208
65–74 12,224
75+ 21,179

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 ATRIAL FIBRILLATION 3,970
2 DYSPNOEA 3,598
3 CEREBROVASCULAR ACCIDENT 3,508
4 THROMBOSIS 2,806
6 CARDIAC DISORDER 2,509
7 DEATH 2,332
8 FALL 2,287
9 FATIGUE 2,193
10 DIZZINESS 1,929
11 ANAEMIA 1,910
12 DIARRHOEA 1,768
13 NAUSEA 1,679
14 ACUTE KIDNEY INJURY 1,673
16 HEADACHE 1,591
17 COVID-19 1,555

Reactions in Death Reports

DEATH 2,331
PNEUMONIA 296
FALL 280
ACUTE KIDNEY INJURY 276
DYSPNOEA 268
CEREBRAL HAEMORRHAGE 262
CARDIAC FAILURE 247
CARDIAC ARREST 214
ANAEMIA 192
COMPLETED SUICIDE 190

Reactions in Hospitalization Reports

DYSPNOEA 2,426
ATRIAL FIBRILLATION 1,760
ANAEMIA 1,600
FALL 1,576
ACUTE KIDNEY INJURY 1,394
FATIGUE 1,167
DIZZINESS 1,098
GASTROINTESTINAL HAEMORRHAGE 1,048
PNEUMONIA 1,047
HYPOTENSION 1,042

Source: FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation

Serious Warnings

Apixaban has two important warnings. First, stopping apixaban too early can raise your risk of blood clots. Don't stop taking it without talking to your doctor. Second, if you have spinal anesthesia or a spinal puncture while taking apixaban, you could get a blood clot around your spine, which can cause long-term paralysis.

Known Drug Interactions

moderate clopidogrel

APPRAISE-2, a placebo-controlled clinical trial of apixaban in high-risk, post-acute coronary syndrome patients treated with aspirin or the combination of aspirin and clopidogrel, was terminated early due to a higher rate of bleeding with apixaban compared to placebo.

Mechanism: Both of these medicines prevent blood clots in different ways, and using them together significantly increases your risk of serious bleeding. Clinical trials were even stopped early because this combination caused too much bleeding.

moderate aspirin

7.3 Anticoagulants and Antiplatelet Agents Coadministration of antiplatelet agents, fibrinolytics, heparin, aspirin, and chronic NSAID use increases the risk of bleeding. APPRAISE-2, a placebo-controlled clinical trial of apixaban in high-risk, post-acute coronary syndrome patients treated with aspirin or the combination of aspirin and clopidogrel, was terminated early due to a higher rate of bleeding with apixaban compared to placebo. In ARISTOTLE, concomitant use of aspirin increased the bleeding risk on apixaban from 1.8% per year to 3.4% per year and concomitant use of aspirin and...

Mechanism: Aspirin and apixaban both thin the blood, and taking them together can nearly double your risk of having a bleeding event. This happens because both drugs make it harder for your blood to clot.

moderate warfarin

In ARISTOTLE, concomitant use of aspirin increased the bleeding risk on apixaban from 1.8% per year to 3.4% per year and concomitant use of aspirin and warfarin increased the bleeding risk from 2.7% per year to 4.6% per year.

Mechanism: Both medications are powerful blood thinners, and using them at the same time greatly increases the risk of dangerous bleeding. Combining these drugs makes it much more difficult for your body to stop any bleeding that starts.

7.2 Combined P-gp Strong CYP3A4 Inducers Avoid concomitant use of apixaban tablets with combined P-gp and strong CYP3A4 Inducers (e.g., rifampin, carbamazepine, phenytoin, St.

Mechanism: Carbamazepine makes your body break down apixaban too fast, which lowers the drug levels in your blood. This makes the medicine less effective at preventing dangerous blood clots.

moderate rifampin

7.2 Combined P-gp Strong CYP3A4 Inducers Avoid concomitant use of apixaban tablets with combined P-gp and strong CYP3A4 Inducers (e.g., rifampin, carbamazepine, phenytoin, St.

Mechanism: Rifampin speeds up the process of removing apixaban from your body. This can leave you with too little medicine to prevent a stroke or blood clot.

Check all your medications →

This is a plain-language summary of FDA-label interaction records and does not provide individual medication-combination directions.

Common Questions

Can I take aspirin with apixaban?
Taking aspirin with apixaban can increase your risk of bleeding. Talk to your doctor before taking aspirin or other pain relievers.
What should I do before surgery?
Tell your doctor that you are taking apixaban before any surgery or procedure. You may need to stop taking it for a short time before the procedure.
Can apixaban be reversed?
Yes, there is a medicine that can reverse the effects of apixaban if you have serious bleeding.
Will apixaban interact with other medicines I'm taking?
Yes, some medicines can affect how apixaban works. Tell your doctor about all the medicines you take, including over-the-counter drugs and supplements.
How long will I need to take apixaban?
The length of time you need to take apixaban depends on why you are taking it. Your doctor will tell you how long to take it.
Can I drink alcohol while taking apixaban?
Talk to your doctor about drinking alcohol while taking apixaban. Alcohol can increase your risk of bleeding.
What if I have kidney problems?
If you have kidney problems, your doctor may need to adjust your dose of apixaban.
What are the signs of bleeding I should watch out for?
Watch out for signs of bleeding, such as unusual bruising, nosebleeds, bleeding gums, blood in your urine or stool, or coughing up blood.
Can I get a rash from apixaban?
Hypersensitivity reactions such as rash are possible, but not common. Seek medical attention if you develop a rash, itching, or swelling.
Does apixaban come in different strengths?
Yes, apixaban comes in 2.5 mg and 5 mg tablets.
What are the common side effects of apixaban?
The registry lists Bleeding more easily (like nosebleeds or heavier periods), Bruising more easily among the most-reported FAERS reaction terms for apixaban. The compiled record contains 62,650 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does apixaban interact with other medications?
The registry has 12 documented interaction rows for apixaban. Notable source-record pairings include clopidogrel, aspirin, warfarin. These rows are not a complete medication review.
What drug class is apixaban?
apixaban belongs to the Direct Oral Anticoagulant (Factor Xa Inhibitor) drug class. It requires a prescription (Rx). Apixaban is used to lower the chance of stroke in people with an irregular heartbeat called atrial fibrillation.
What pregnancy or breastfeeding source fields are listed for apixaban?
The FDA label for apixaban contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.

Other drugs grouped near apixaban - same-class peers and common alternatives.

Compare apixaban vs aspirin side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for apixaban: nearest FDA FAERS report volume and nearest death-report share among drugs with at least 1,000 logged reports, excluding same-class neighbors listed above. Counts reflect reporting volume, not proven individual harm.

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What the FDA Data Shows for apixaban

The FDA label for apixaban (sold under brand names such as Eliquis) classifies it as a prescription-only medication in the Direct Oral Anticoagulant (Factor Xa Inhibitor) class. Apixaban is used to lower the chance of stroke in people with an irregular heartbeat called atrial fibrillation. Official labeling lists 2 commonly reported side effects, including Bleeding more easily (like nosebleeds or heavier periods), Bruising more easily.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 62,650 voluntary reports. The database also lists 12 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated moderate severity. NADAC pricing from CMS.

Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information are separate source-record fields. This page is a public FDA/CMS registry and does not provide medical, treatment, substitution, or medication-change directions.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. This registry does not provide medication decisions.

Last updated: June 15, 2021

PlainMeds is rendered directly from FDA openFDA/FAERS extracts, DailyMed labels, and CMS drug-pricing files, no number is typed in by an editor. FAERS counts, recalls, shortages, and price figures on this page are queried live from those federal extracts. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of 2026-05-15. Primary sources: openFDA / FAERS, DailyMed and CMS Part B ASP.

Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled from the source snapshot dated . See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a data issue.

All federal data sources used on this page