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Learn more about the history of Tasigna® and the alleged failures of its parent company Novartis®
Tasigna® (nilotinib) is a prescription drug that is used to treat chronic myeloid leukemia (CML).
CML is a type of cancer that originates in the bone marrow and enters the blood–it accounts for about 15% of all adult leukemia cases.
Tasigna® is a relatively new drug that was developed by Novartis® and approved for use in the treatment of CML in 2007–it works by blocking certain proteins that cause leukemia cancer cells to grow.
Since its original release, Tasigna® has become a very profitable drug for Novartis®–however, not long after Tasigna® was first released, adverse incident reports and other evidence began to appear indicating that the drug could be causing serious cardiovascular problems in some patients.
In 2011, the results of several studies reported that the use of Tasigna® was causing some patients to develop accelerated atherosclerosis–a condition in which the arteries delivering blood from the heart become hardened and narrow.
Normally, atherosclerosis is something that can develop gradually over time as a person gets older–however, the use of Tasigna® was causing certain patients to develop atherosclerosis within a few months.
Atherosclerosis can be very dangerous as it can result in serious cardiac and vascular events such as heart attack, or peripheral arterial disease.
Novartis® amended its Canadian prescribing information to include a warning that Tasigna® can cause rapidly evolving vascular disease–however, Novartis® allegedly deliberately chose not to add this warning to the prescribing information label for Tasigna® in the U.S.
In fact, the U.S. drug label for Tasigna® still does not contain any information about the risk of atherosclerosis.
Under certain circumstances, victims who suffer from unmarked Tasigna® side effects can pursue compensation for their losses.
Learn about Tasigna®-induced atherosclerosis and the potential for claiming compensation
The medical literature suggests a strong probability that Tasigna® is linked to atherosclerotic-related events, including stroke.
While many patients taking Tasigna® are at a higher risk for atherosclerosis, the connection in many cases will be obvious because the medical literature describes an association between Tasigna® and a rare form of accelerated atherosclerosis.
According to the research concerning Tasigna®-induced atherosclerosis:
- Atherosclerosis generally develops over an extended time, taking years to become an acute risk.
- Rapid progression or sudden aggravation of atherosclerosis is uncommon.
- Tasigna®-induced atherosclerosis often develops much more quickly, giving doctors less time to diagnose and combat the condition.
A growing number of people who developed rapid atherosclerosis from using Tasigna® and suffered serious injuries have filed lawsuits against Novartis®.
The lawsuits allege that Novartis® allegedly knew as early as 2010–and probably earlier–that Tasigna® caused accelerated atherosclerosis and related conditions.
Novartis® allegedly knowingly and intentionally failed to warn about these risks in the U.S. in order to protect its financial interests.
August 2021 Update: On August 12, 2021, the United States Judicial Panel on Multidistrict Litigation ordered the creation of a Tasigna® class action lawsuit for claims involving this therapy.
December 2021 Update: A new study published this fall in the journal of Cardiology-Oncology identified a clear link between the use of Tasigna® and vasospastic angina–this is yet another potentially dangerous side-effect linked to the low blood flow problems caused by Tasigna®.
The USA Justice Group encourages those suffering after taking Tasigna® to request a free, private case evaluation for justice and compensation!
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Depending on the circumstances, the case could be filed for potential compensation
Please seek the advice of a medical professional before making health care decisions. This advertisement is not associated with Tasigna® or any government agency.
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