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apixaban

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Brand names: Eliquis

Direct Oral Anticoagulant (Factor Xa Inhibitor) Rx

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 →

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.

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.

How to Take It

Take apixaban exactly as your doctor tells you. For most people with atrial fibrillation, the usual dose is 5 mg twice a day. If you are older than 80, weigh less than 132 pounds, or have kidney problems, your doctor may prescribe 2.5 mg twice a day. For DVT/PE treatment, you'll likely take 10 mg twice a day for 7 days, then 5 mg twice a day.

Pregnancy & Breastfeeding

Apixaban is not recommended during pregnancy because it may increase the risk of bleeding during pregnancy and delivery. Talk to your doctor about the risks and benefits of taking apixaban if you are breastfeeding. You may need to stop taking the drug or stop nursing.

Missed Dose

If you miss a dose of apixaban, take it as soon as you remember on the same day. Then, continue taking it twice a day as usual. Do not double your dose to make up for the missed one.

Storage

Store apixaban at room temperature, between 68°F and 77°F.

Side Effects (from patient reports)

Based on 27,825 FDA adverse event reports.

Irregular heartbeat
3,970
Shortness of breath
3,598
Stroke
3,508
Blood clot
2,806
Using the medicine for something it's not approved for
2,693
Heart problem
2,509
Death
2,332
Fall
2,287
Tiredness
2,193
Feeling lightheaded
1,929

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

Death-Related Reports

6,759

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
5 OFF LABEL USE 2,693
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
15 DRUG INEFFECTIVE 1,636

Reactions in Death Reports

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

Reactions in Hospitalization Reports

DYSPNOEA 2,426
ATRIAL FIBRILLATION 1,760
ANAEMIA 1,600
FALL 1,576
ACUTE KIDNEY INJURY 1,394
OFF LABEL USE 1,338
FATIGUE 1,167
DIZZINESS 1,098
GASTROINTESTINAL HAEMORRHAGE 1,048
PNEUMONIA 1,047

Source: FDA FAERS (Adverse Event Reporting System) 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.

What to do: Use this combination only if specifically directed by your doctor and watch for any signs of unusual bruising or bleeding. Your healthcare provider should monitor you very closely.

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 warfa...

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.

What to do: Your doctor should monitor you closely for bleeding while you are on both medications. Do not start or stop taking aspirin without first consulting your healthcare provider.

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.

What to do: Avoid taking these two blood thinners together unless your doctor tells you it is absolutely necessary. You will need frequent monitoring and blood tests to ensure your safety.

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.

What to do: Avoid taking these two medicines together. Talk to your doctor about using a different treatment.

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.

What to do: Do not use these medications at the same time. Your healthcare provider will likely need to choose an alternative medicine.

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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 most commonly reported side effects of apixaban include Bleeding more easily (like nosebleeds or heavier periods), Bruising more easily. Based on 27,825 FDA adverse event reports. Always consult your healthcare provider about potential side effects.
Does apixaban interact with other medications?
Yes, apixaban has 12 known drug interactions. Notable interactions include clopidogrel, aspirin, warfarin. Always inform your doctor about all medications you are taking.
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.
Is apixaban safe during pregnancy?
Apixaban is not recommended during pregnancy because it may increase the risk of bleeding during pregnancy and delivery. Talk to your doctor about the risks and benefits of taking apixaban if you are breastfeeding. Always consult your healthcare provider before using any medication during pregnancy or breastfeeding.

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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 27,825 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 further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice — always consult a licensed healthcare provider before starting, stopping, or changing any medication.

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. Always consult a healthcare professional before making medication decisions.

Last updated: June 15, 2021

All federal data sources used on this page