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Rea, Delphine, et. al.

Lots of folks who call us with Tasigna cases have questions about the drug and the lawsuits we are now filing.

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Patients were not adequately warned about the danger of resultant or atherosclerosis vascular disease.

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One of the major pieces of research linking Tasigna with atherosclerosis discovered some patients taking the drug experienced vascular problems and was printed in 2011.

Novartis was represented by Evan R. Chesler, Rachel G. Skaistis and Benjamin Gruenstein of Cravath, Swaine, & Moore in New York.

All persons who suffered serious side effects and obtained Tasigna are entitled to get a free case review from the Tasigna attorneys.

Chronic Myeloid Leukemia Drug Tasigna Associated with Arteriosclerosis and Wrongful Death.


88, no.

In the lawsuit, Kester asserts that Novartis defrauded the Medicare and Medicaid programs by illegally paying kickbacks to pharmacies so that they would recommend to physicians and patients six of Novartis’ specialty medications — the oncology medications Exjade, Gleevec and Tasigna, the organ transplant, immunosuppressant drug Myfortic, and the cystic fibrosis drugs TOBI and TOBI Podhaler.

Nor did Novartis properly warn of the atherosclerosis-related risks on the United States Tasigna label,” the complaint alleges.

The Novartis company is the person who’s responsible for marketing and the manufacturing of medication.

Atherosclerosis can lead to other diseases, such as: Likewise, studies have indicated tyrosine kinase inhibitors and a link between Tasigna and events.

On April 9, 2013, Health Canada (the Canadian equivalent to the U.S. Food and Drug Administration) published a statement to healthcare providers alerting them to the possibility for Tasigna to cause atherosclerosis-related diseases.

Research indicates a link between the use of Tasigna to treat chronic myeloid leukemia (CML) and atherosclerosis, a disorder which causes the arteries to harden and thicken due to the buildup of plaque.

This page provides answers to common Tasigna lawsuit questions that apply to claims that are atherosclerosis from Virginia.

” The lawsuit was filed on March 22, 2016 in the U.S. District Court for the Eastern District of California — In RE: Lauris, et al. v.

Doctors were advised to track their Tasigna patients for signs of the artery disease.

We’ll be delighted answer your questions as as possible and to go over your circumstances in detail.

After a review revealed that 277 reports of this condition was logged with the Novartis global safety database between January 1st, 2005 and January 31, 2013 the label for Tasigna was updated to notice a risk of arteriosclerosis.

It’s believed thousands of patients might have been affected as a result.

To access your own free consultation, use the online chat feature or contact form on this website.

Research suggests a link between atherosclerosis and the cancer drug, a serious disorder which causes the arteries to harden as a result of the buildup of plaque.

Chemotherapy drug Tasigna (nilotinib) linked to serious side effects including coronary artery disease (CAD), atherosclerosis, hardening/narrowing of the arteries, restricted blood flow, heart failure, limb amputations, death.

The thickening is due to a buildup of white blood cells and the development of a plaque.

Within 5 years of Tasigna entering the U.S. market, researchers started noting higher than expected number of reports of peripheral arterial diseases (PAD) in cancer patients treated with the medication.

Health Hazards of Atherosclerosis.


The Pharmaceutical Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in Tasigna lawsuits.

Tasigna Removed From 2018 Drug Formulary Lists.

The Tasigna lawsuit was filed by the family of Dennis Lauris, a man from California who took Tasigna and died of atherosclerosis.

According to an article in HarrisMartin’s Drugs & Medical Devices Publication, the family of a California man claims that their deceased loved one died from an atherosclerosis-related condition and that Novartis failed to warn physicians and patients in the U.S. about dangerous side effects linked to the medication.

Many related studies were published in peer-reviewed jounrals in Europe, Canada and the USA in the years.