Pradaxa Lawsuit and Side Effects Information
Pradaxa is a prescription medication that is designed to reduce the risk of stroke and the development of blood clots in individuals diagnosed with atrial fibrillation. The medication is only approved for use in cases of atrial fibrillation that are not caused by a problem with the heart's valves. Atrial fibrillation is a heart condition that causes an abnormal heart rhythm, which occurs as a result of a malfunction in the heart's electrical system. When the heart does not beat normally, an individual is at an increased risk of developing a dangerous blood clot that could lead to a stroke.Other resources: Injured in Tucson? Visit Goldberg & Osborne's Tucson page today.
Clinical studies have found Pradaxa to be more effective at reducing the risk of stroke when compared to warfarin, which is another commonly prescribed blood thinner or anticoagulant. The primary goal of treatment with Pradaxa is to prevent blood clots from developing.
How Pradaxa Works
Pradaxa is classified as a direct thrombin inhibitor and works by preventing blood from clotting. This is accomplished by inhibiting the effects of thrombin, which is a protein in the body that is responsible for the clotting of blood. By blocking the ability of thrombin to clot blood, the formation of a serious blood clot is significantly reduced.
Pradaxa dosage is largely dependent on how well a patient's kidneys are functioning and other medications they are taking. The standard dosage for Pradaxa is 150 mg twice each day for individuals who have healthy kidneys. A lower dosage of 75 mg is prescribed for individuals whose kidney function has somewhat diminished.
Pradaxa can be taken with or without food and there are no dietary restrictions associated with it. The capsules should be swallowed whole and never crushed or chewed. If a dosage is missed, it can be taken as soon as the patient remembers unless the next scheduled dose is less than six hours away. If a patient suddenly stops taking Pradaxa, they are at an increased risk of stroke. Patients should only stop taking Pradaxa under the direction of their physician.
An extra capsule of Pradaxa should not be taken in the event of a missed dose. Doing so can result in a life-threatening overdose, which may cause extensive bleeding. If an overdose does occur, an individual should seek emergency care as soon as possible. It may be possible to prevent complications caused by an overdose if it is caught early.
The Pradaxa capsules should be stored in their original container or blister packaging until ready to use and not placed in a pill organizer or box. The bottle should be tightly closed and stored in a location that is at room temperature and away from moisture and excessive heat. An opened bottle of Pradaxa should be used within four months.
Drug Interactions and Pradaxa Lawsuits
It is essential that patients inform their doctor of all over-the-counter and prescription medications, herbal supplements and vitamins they are currently using before taking Pradaxa, particularly those that treat or prevent blood clots. It is possible that certain medicines may alter the way in which Pradaxa works or increase the risk of side effects.
Patients taking medications such as aspirin, warfarin sodium, heparin, nonsteroidal anti-inflammatory drugs (NSAIDs), prasugrel, clopidogrel or dronedarone must ask their doctor if it is safe for them to take Pradaxa. These types of medications significantly increase the risk of bleeding when taken with Pradaxa. If someone you know was injured as a result of taking Pradaxa, you may have a case. Speaking to a Pradaxa lawsuit lawyer is the only way to learn about your rights.
Although Pradaxa is often a life-saving medication for many individuals, it does pose the risk of serious and potentially deadly side effects. The most common side effects associated with Pradaxa include indigestion, stomach pain, diarrhea, nausea and heartburn. These types of gastrointestinal problems have been reported by up to 35 percent of individuals who take Pradaxa.
Bleeding is another serious side effect that may occur. Since Pradaxa is a blood thinner or anticoagulant, it raises the risk of bleeding for users of the medication. Nearly 16 percent of patients taking Pradaxa have experienced bleeding, with up to three percent of users reporting serious bleeding. Signs of bleeding can include nosebleeds, unusual or easy bruising, low blood pressure, coughing up blood and blood in urine or stool.
Although rare, it is possible for some individuals to develop a severe allergic reaction to Pradaxa. This can produce symptoms such as rash, difficulty breathing, hives, itching, wheezing and swelling of the throat or mouth. Other serious side effects include weakness, vision problems, chest pain, joint pain and vomiting. Patients should seek medical attention immediately if any of these side effects occur.
Warnings and Precautions
Risk of bleeding may be higher in patients who are over the age of 75, have a stomach ulcer or recurring bleeding of the stomach or intestines and have an existing kidney problem. Since Pradaxa prevents blood from coagulating, activities that may cause injury or bleeding should be avoided while taking Pradaxa. Even a minor injury can cause excessive bleeding. Patients should not consume alcohol while taking Pradaxa as this may raise the risk of bleeding within the intestines or stomach.
If a patient requires any type of dental or medical procedure or surgery, they may need to stop taking Pradaxa for one or more days since this poses a dangerous bleeding risk. This should be discussed with a physician given the potential risks involved when an individual suddenly stops taking Pradaxa.
Anyone with a condition that causes unusual bleeding such as an intestinal ulcer, bleeding in the brain or a bleeding stomach should not take Pradaxa. Individuals who have had a previous allergic reaction to any ingredient in Pradaxa should inform their physician and not take the medication. Kidney function may need to be checked before beginning treatment with Pradaxa and periodically while under treatment. If you're thinking about filing a Pradaxa lawsuit, speak witha lawyer today to learn about your rights.
Pradaxa and Pregnancy
The effects that Pradaxa may have on a fetus are not currently known. While animal studies have indicated complications if Pradaxa is taken during pregnancy, it is unknown if these adverse effects can be seen in humans. If a woman taking Pradaxa is planning on becoming pregnant or is currently pregnant, she should discuss the potential benefits and risks of taking the drug during pregnancy. If the benefits of taking Pradaxa over the course of pregnancy outweigh the potential risks, it may be possible for pregnant women to continue taking Pradaxa.
Pradaxa and Breastfeeding
Since research has not been conducted investigating if Pradaxa can reach an infant through breast milk, it is difficult to determine if it is safe to use while breastfeeding. Women should exercise caution if planning to breastfeed while under treatment with Pradaxa and may want to consider avoiding breastfeeding.
Pradaxa Lawsuit Information
The only way to know if you have a case is to speak with an experienced lawyer today regarding your possible Pradaxa lawsuit. Click the image below to fill out our form.