Tasigna Drug Warning for Peripheral Arterial Disease
Leukemia studies show that the anti-cancer drug Tasigna indicate adverse side effects reactions in treated patients
Friday, June 30, 2017 - Peripheral Artery Disease has been reported in alarming numbers by people who have taken Tasigna to treat Philadelphia chromosome-positive chronic myeloid leukemia. Studies into the anti-cancer drug Tasigna indicate that the side effects of the taking the drug can be deadlier than the disease the drug was intended to cure. One such insidious side effect of Tasigna is Peripheral Artery Disease that can lead to amputations of the foot and even an entire leg due to infections and tissue necrosis. The extremities of the body rely on major arteries to carry oxygen-rich blood and when a person develops Peripheral Artery Disease, plaque builds up in the artery and reduces or entirely cuts off this necessary blood flow and its critical nutrients. In addition to tissue necrosis and amputation, other patients have had heart attacks and strokes and this has led the United States Food and Drug Administration to require Tasigna to carry a "Black Box" warning, the most severe, alerting consumers to these dangers.
Peripheral Artery Disease was not included in the Tasigna warnings in the United States.
Cancer physicians and other cancer health care professionals in the United States were misled for years after the risks of atherosclerosis and Peripheral Artery Disease was stated by the Canadian health agency, Health Canada but not in the US. This negligence in providing American regulatory agencies with the necessary facts resulted in many thousands of Tasigna patients being stricken with irreversible Peripheral Artery Disease, having heart attacks, strokes, and even deaths. In addition, the drug's maker and marketer, Swiss-based pharmaceutical giant Novartis International AG, deliberately took steps to protect its $1.7 billion annual Tasigna market monopoly in the US by aggressively marketing the drug as a "superior" alternative to other cancer treatments in printed brochures and on social media platforms when in fact there is no proof of that claim. As a result, the US Justice Department sued Novartis winning a $390 million settlement claiming that the company exaggerated its claims of the drug's effectiveness, misbranded the drug, and paying physicians illegal incentives in the form of cash rebates and bonuses to use Tasigna instead of other, safer alternatives. Even today, cancer doctors are warned to test prospective patients for signs of peripheral artery disease before, during and after the application of Tasigna cancer chemotherapy. Prospective Tasigna patients should undergo an electrocardiogram (ECG) to test for an irregular heartbeat or other signs of heart abnormality.
Compassionate Legal Representation for Tasigna Victims
The Law Firm of Onder, Shelton, O'Leary & Peterson, LLC, represent Tasigna cancer clients from across the nation who have suffered Peripheral Artery Disease and other health complications from using the much maligned, anti-cancer drug Tasigna. Onder Law has won million dollars in settlements for plaintiffs successfully suing large pharmaceutical companies such as Johnson & Johnson and others that have willfully chosen to put profits ahead of consumer safety. Our clients have received reimbursement of their medical expenses, lost wages, pain, and suffering and all other related damages. If you have been given the anti-cancer chemotherapy treatment Tasigna, and experienced adverse side effect and were not warned in advance, call St. Louis-based Onder, Shelton, O'Leary & Peterson, LLC, today.
More Recent Tasigna Atherosclerosis Lawsuit News:
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- Tasigna's Atherosclerosis Risk Is Well-Documented By Researchers For Peer-Reviewed Medical Publications | 5/8/2019
- Tasigna's Atherosclerosis Side Effect Is Not Forgotten | 4/17/2019
- Trying Tasigna As A Last Resort May Make Sense To Terminally Ill Cancer Patients | 4/12/2019
- Novartis Claim Tasigna Can Help Parkinson's Patients is Met With Skepticism | 4/4/2019
- Novartis Failed To Warn American Doctors Who In Turn Failed To Warn Patients of Tasigna's Atherosclerosis Risks | 3/20/2019
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- Some Patient Can Cease Taking Tasigna But They May Have Already Developed Atherosclerosis | 3/12/2019
- Health Experts Warn of Potentially Deadly Tasigna Drug Interactions | 3/5/2019
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- Tasigna Studies Show The Drug Should Be Taken As A Last Resort | 2/24/2019
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- Novartis Has a History of Deceptive Sale Practices That Taints Their Credibility | 1/22/2019
- Novartis Changes Tasigna's Label But Not Its Toxicity | 1/16/2019
- Tasigna Doctors May Be Ignoring Atherosclerosis Risks | 1/11/2019
- Cancer Doctors Prescribing Tasigna Should Be Trained Like Heart Specialists | 1/8/2019
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- Early Warning Signs of Chronic Myeloid Leukemia (CML) | 12/5/2018
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- Novartis Fraudulent Marketing Deception | 5/29/2018
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- Novartis Tasigna Anti-Cancer Drug Has Side Effects That Include Sudden Death | 5/22/2018
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- Who Can Be Considered A Tasigna Victim | 8/4/2017
- Novartis AG makers of Tasigna Failed to Warn Public of the Dangerous Side Effects | 7/14/2017
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- Novartis International AG Lawsuits | 6/23/2017
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- Tasigna Lawsuits Against Drug Makers Novartis | 6/16/2017
- Atherosclerosis of the Aorta Linked to Tasigna Anti-Cancer Drug | 6/12/2017
- Makers of Tasigna Leukemia Drug Lawsuit | 6/9/2017
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Lawyers for Tasigna Atherosclerosis Lawsuits
Attorneys handling Tasigna lawsuits for leukemia, non-Hodgkin lymphoma, and multiple myeloma offer free, no-obligation case review for individuals and families who believe they may have grounds to file a Tasigna lawsuit. Working on a contingency basis, these attorneys are committed to never charging legal fees unless they win compensation in your Tasigna lawsuit. The product liability litigators handling Roundup claims at the Onder Law Firm have a strong track record of success in representing families harmed by dangerous drugs and consumer products.