UNDERSTANDING AFIB

Understanding Afib

  • AFIB & STROKE
  • UNDERSTANDING AFIB
  • AFIB & STROKE RISK

Let’s start with the basics. What is atrial fibrillation (or AFib as it’s often called)? And who gets it?

AFib is a type of irregular heartbeat. It occurs when one or both of the upper chambers of the heart—called the atria—beat erratically. This puts them out of sync with the heart's 2 lower chambers—called the ventricles.

AFib affects more than 2 million people in the United States. The odds of developing AFib go up with age. In fact, the American Heart Association states that AFib is the most common serious type of irregular heartbeat in people over age 65. It's also sometimes associated with other health problems, such as heart disease, diabetes, or high blood pressure.

WHAT COULD HAVING THIS DISORDER MEAN FOR ME?

Some of the signs of AFib include:

  • Racing, irregular heartbeat
  • Fluttering in the chest
  • Heart palpitations
  • Dizziness
  • Shortness of breath
  • Chest pain
  • Weakness
  • Faintness
  • Fatigue when exercising
  • Sweating

However, in some people, AFib may cause no symptoms at all.

This is why, as for many people, your doctor may have discovered that you have AFib during a routine physical exam or testing for another condition. Your doctor most likely confirmed your diagnosis through a thorough physical exam and medical history. He or she also likely used an electrocardiogram (EKG) and other tests to look for the underlying cause of the disorder and any complications.

You should know that having AFib puts you at a nearly 5 times greater risk of a stroke than if you don't have it. Even if you have no symptoms.

Click on the link below to learn why—and what you can do about it.

NEXT: Learn more about the relationship between AFib and stroke 

SEND TO A FRIEND

Create a personalized doctor discussion guide. And help make sure you get the answers you need about AFib not caused by a heart valve problem, stroke, and treating with PRADAXA.

CREATE YOUR GUIDE 

In a clinical trial, PRADAXA 150 mg capsules reduced the risk of stroke 35% more than warfarin. Risk reduction was greatest when compared to patients on warfarin whose blood tests showed lower levels of control.

LEARN MORE 

WHAT IS PRADAXA?

PRADAXA is a prescription blood-thinning medicine used to reduce the risk of stroke and blood clots in people with atrial fibrillation not caused by a heart valve problem. With atrial fibrillation, part of the heart does not beat the way it should. This can cause blood clots to form, increasing your risk of a stroke. PRADAXA lowers the chance of blood clots forming in your body.

 

IMPORTANT SAFETY INFORMATION ABOUT PRADAXA

PRADAXA can cause bleeding which can be serious and sometimes lead to death. Don’t take PRADAXA if you currently have abnormal bleeding or if you have ever had an allergic reaction to it.

Your risk of bleeding with PRADAXA may be higher if you:

  • • are 75 years old or older
  • • have kidney problems
  • • have stomach or intestine bleeding that is recent or keeps coming back or you have a stomach ulcer
  • • take other medicines that increase your risk of bleeding, like aspirin products, non-steroidal anti-inflammatory drugs (NSAIDs) and blood thinners
  • • have kidney problems and take dronedarone (Multaq®) or ketoconazole tablets (Nizoral®)

Call your doctor or seek immediate medical care if you have any of the following signs or symptoms of bleeding:

  • • any unexpected, severe, or uncontrollable bleeding; or bleeding that lasts a long time
  • • unusual or unexpected bruising
  • • coughing up or vomiting blood; or vomit that looks like coffee grounds
  • • pink or brown urine; red or black stools (looks like tar)
  • • unexpected pain, swelling, or joint pain
  • • headaches and feeling dizzy or weak

It is important to tell your doctor about all medicines, vitamins and supplements you take. Some of your other medicines may affect the way PRADAXA works.

Take PRADAXA exactly as prescribed by your doctor. Don’t stop taking PRADAXA without talking to your doctor as your risk of stroke may increase.

Tell your doctor if you are planning to have any surgery, or medical or dental procedure, because you may have to stop taking PRADAXA for a short time.

PRADAXA can cause indigestion, stomach upset or burning, and stomach pain.

Click here for full Prescribing Information including Medication Guide

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call
1-800-FDA-1088.

The health information contained in this Website is provided for educational purposes only and is not intended to replace discussions with a healthcare professional. All decisions regarding patient care must be made with a healthcare professional, considering the unique characteristics of the patient.

IMPORTANT SAFETY INFORMATION ABOUT PRADAXA

PRADAXA can cause bleeding which can be serious and sometimes lead to death. Don’t take PRADAXA if you currently have abnormal bleeding or if you have ever had an allergic reaction to it.


Your risk of bleeding with PRADAXA may be higher if you:

  • • are 75 years old or older
  • • have kidney problems
  • • have stomach or intestine bleeding that is recent or keeps coming back or you have a stomach ulcer
  • • take other medicines that increase your risk of bleeding, like aspirin products, non-steroidal anti-inflammatory drugs (NSAIDs) and blood thinners
  • • have kidney problems and take dronedarone (Multaq®) or ketoconazole tablets (Nizoral®)

Call your doctor or seek immediate medical care if you have any of the following signs or symptoms of bleeding:

  • • any unexpected, severe, or uncontrollable bleeding; or bleeding that lasts a long time
  • • unusual or unexpected bruising
  • • coughing up or vomiting blood; or vomit that looks like coffee grounds
  • • pink or brown urine; red or black stools (looks like tar)
  • • unexpected pain, swelling, or joint pain
  • • headaches and feeling dizzy or weak

It is important to tell your doctor about all medicines, vitamins and supplements you take. Some of your other medicines may affect the way PRADAXA works.


Take PRADAXA exactly as prescribed by your doctor. Don’t stop taking PRADAXA without talking to your doctor as your risk of stroke may increase.


Tell your doctor if you are planning to have any surgery, or medical or dental procedure, because you may have to stop taking PRADAXA for a short time.


PRADAXA can cause indigestion, stomach upset or burning, and stomach pain.



WHAT IS PRADAXA?


PRADAXA is a prescription blood-thinning medicine used to reduce the risk of stroke and blood clots in people with atrial fibrillation not caused by a heart valve problem. With atrial fibrillation, part of the heart does not beat the way it should. This can cause blood clots to form, increasing your risk of a stroke. PRADAXA lowers the chance of blood clots forming in your body.


Click here for full Prescribing Information including Medication Guide.


You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.


The health information contained in this Website is provided for educational purposes only and is not intended to replace discussions with a healthcare professional. All decisions regarding patient care must be made with a healthcare professional, considering the unique characteristics of the patient.



Your request is processing, please wait one moment...

FOR HEALTHCARE PROFESSIONALS

close
This site is intended for US healthcare
professionals only. Would you like to continue?

YES, I am a US
healthcare professional.

US

I am a healthcare professional but
am located in one of these countries

  • Spain
  • Sweden
  • Germany
  • Italy
  • Netherlands
For all other countries, click here.
NO, I am not a healthcare professional.
CLOSE X

Please Note: You are now leaving a Boehringer Ingelheim Pharmaceuticals. Inc., site. Boehringer Ingelheim Pharmaceuticals. Inc., has not reviewed the contents of all the pages and sites that may be linked to this site. Boehringer Ingelheim Pharmaceuticals. Inc., is not responsible and disclaims any liability to the content of any other page or site or for any viruses or similar harmful programs that may be present on such pages or sites. Linking to any other page or site is at your own risk.

PRADAXA® (DABIGATRAN ETEXILATE MESYLATE) CAPSULES:
IMPORTANT STORAGE AND HANDLING INFORMATION
PRADAXA must be kept dry. To protect it from moisture, PRADAXA comes in either a bottle with a special cap that contains a drying agent or a blister pack with each capsule sealed separately.

When taking PRADAXA, please follow these instructions carefully:
  • Always store PRADAXA in its original container.
    • Never put PRADAXA into any other container, such as a pill box or pill organizer.
    • Store PRADAXA at room temperature between 59°F to 86°F (15°C to 30°C).
  • If your PRADAXA came in a bottle:
    • Be sure the closure tape, which indicates that the bottle has not been opened, is intact when you receive your prescription. Do not remove the closure tape until you are ready to open the bottle. Open your new bottle only after finishing your current bottle.
    • Once the bottle is opened, you must use PRADAXA within 30 days.
      • As soon as you open the bottle, write the date on the label. PRADAXA will expire 30 days after the date you opened the bottle.
      • Do not alter the child-proof cap.
      • Safely throw away any unused PRADAXA after 30 days.
      • If your pharmacist or other healthcare provider gave you more than one bottle of PRADAXA, be sure to open only one bottle at a time.
    • Each time you take PRADAXA:
      • Remove only one capsule from the opened bottle.
      • Immediately and tightly close the bottle.
  • If your PRADAXA came in a blister pack, remove only one capsule from the pack at a time.
  • Always read the Medication Guide included with each of your PRADAXA prescriptions. There may be information that is new or that has changed since your last prescription.
  • Remember to keep PRADAXA, and all medicines, out of the reach of children.
Not actual size

Print
Close