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FDA to Conduct Pradaxa Study

The US Food and Drug Administration (FDA) has announced a plan to conduct a safety assessment of the blood thinner Pradaxa (dabigatran).  The FDA describes the assessment as “a one-time assessment of selected safety outcomes in adults with atrial fibrillation who are new users of dabigatran or warfarin.”

The study will “assess systematically the rates of bleeding and thromboembolic outcomes associated with the use of dabigatran and warfarin for patients with atrial fibrillation using data from the FDA Mini-Sentinel Distributed Database (MSDD).”

According to the FDA, Mini-Sentinel is a part of the FDA sentinel surveillance system that uses electronic healthcare data from nearly 100 million patients.

Pradaxa manufacturer Boehringer Ingelheim issued a statement following the news of the study announcement saying, “[the] fact that FDA requests and receives data on a particular product through Mini-Sentinel does not necessarily mean there is a safety issue with the product.”

Studies done in other countries have showed that individuals using Pradaxa have roughly a 33 percent higher risk for fatal health risks as compared to individuals using the blood thinner warfarin.

If you have used Pradaxa and have experienced any adverse side effects our defective drug attorneys are on the patients’ side. Contact our injury lawyers toll free at (888) 841-9623 to discuss the Pradaxa lawsuit. Our firm offers confidential, no obligation consultations.

Zoll & Kranz, LLC – Pradaxa attorneys

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Michelle L. Kranz

Michelle is a founding partner of Zoll & Kranz, located in Toledo, Ohio. Michelle has been a plaintiff’s lawyer for the entirety of her practice – over 32 years. She devotes the majority of her time to complex consolidated litigation and class action including advocating for people injured by medical devices, prescription medications, or corporate negligence.

This article has been written and reviewed for legal accuracy and clarity by the team of writers and attorneys at Zoll & Kranz, LLC and is as accurate as possible. This content should not be taken as legal advice from an attorney. If you would like to learn more about our owner and experienced Ohio injury lawyer, Michelle L. Kranz, you can do so here.

Zoll & Kranz, LLC does everything possible to make sure the information in this article is up to date and accurate. If you need specific legal advice about your case, contact us. This article should not be taken as advice from an attorney.

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You can learn more about this topic by visiting any of our Pradaxa Lawsuit pages listed below:
Boehringer Ingelheim Fined $931,000 For Withholding Evidence
Break in Pradaxa Case: Judge Rejects Protective Order from Pharmaceutical Company
Daughters File Pradaxa Lawsuit Over Mother’s Death
Family Files Pradaxa Lawsuit After Woman Suffers Massive Hemorrhaging
FDA Warns Pfizer’s Drug Tygacil Raises Risk of Death
First Phase of Pradaxa Settlement Funds Ordered to Be Set Aside
Has Pradaxa Been Linked to Major Bleeding Events?
How Many Patients Died in a Trial Study of Pradaxa?
Is Pradaxa Safe to Prescribe to Patients?
Loved One Died After Taking Pradaxa? Penn. Widow Files Wrongful Death Lawsuit
Over 2,000 Lawsuits Filed Over Blood Thinner, Pradaxa
Pradaxa Adverse Events Extremely High According to Reporting System
Pradaxa Approved to Treat VTE, Concerns Linger
Pradaxa is the Most Complained About Drug in the Country
Pradaxa Lawsuits Expected to Begin in August
Pradaxa Settlement Announced to be a Potential $650 Million Deal
Should I Take Pradaxa?
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