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Actos is a member of controversial TZD (thiazolidinedione) drug family. Drugs in the TZD family work by increasing the sensitivity of body cells to insulin that is produced by pancreas. The other drugs in the family, Avandia (rosiglitazone and Rezulin (troglitazone), have been restricted of withdrawn from the market due to deadly side effects.  All TZD drugs are generally linked to edema, anemia, heart and liver problems.

Takeda Pharmaceuticals introduced Actos to the market and claimed it was a safe alternative to Avandia. Actos sales skyrocketyed even after studies revealed it increased risk of congestive heart failure and bladder cancer. Suave marketing by Takeda enables it to record stellar sakes records even as researchers delve deeper to drug’s connection to severe health complications.

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After conclusive links between Actos, congestive heart failure, bladder cancer and other debilitating diseases, dozens of patients introduced lawsuits against Takeda. They allege that they were not provided with proper warning about the risks of using Actos. The plaintiffs argue that  they are frightened about bladder cancer in future.  Many turned to court system is to seek compensation for injuries, enormous pain, suffering and ongoing medical bills.

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Legal analysts estimate that there might be up to 10,000 court complaints against Takeda and Actos. The judges presiding over the cases are keen to move them quickly.  So far there are thousands of patients who have been joined together in a Louisiana federal court multidistrict litigation (MDL).

An MDL streamlines and centralizes the discovery process. However it is different from class action where an in individual sues a group of persons, a group sues another or a group sues one person. MDL allows the cases to be heard separately. There are other groups of cases consolidated into mass torts at Illinois and California.

In medical product liability such as the case against Takeda, plaintiffs seek monetary compensation in form of compensatory damages. This is money awarded to replace what plaintiffs lose due to injury. Punitive damages which are monetary amount to punish the defendant can also be awarded.

The plaintiffs against Takeda opted to join MDL or Mass Tort for power of numbers. The difference between the two is that MDL takes place in federal courts and mass tort in state court. Legal procedures allow plaintiffs with similar questions to consolidate under one judge who handles pretrial discovery and other proceedings.  This alternative allows consistency and saves time. In both cases, plaintiffs retain their individual lawsuits and lawyers as each case is heard separately.

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Accutane Lawsuits Continue to Grow Well Into Thousands

Elise Kramer | February 10th, 2012 | Posted in Accutane Crohns Disease News

The Food and Drug Administration has been heavily involved in the investigation of Accutane side effects since it became clear that a number of patients were suffering from a range of serious side effects associated with the acne medication. The Food and Drug Administration released a report addressing these concerns in 2002, outlining the risk of psychiatric side effects and birth defects if taken by a pregnant patient. However, they did not in that report discuss the risk of psychological side effects.

FDA report with no mention of Accutane IBD

Accutane inflammatory bowel disease is now one of the most commonly cited side effects in Accutane lawsuits. Accutane ulcerative colitis and Accutane Crohn’s disease are two conditions that fall under the spectrum of inflammatory bowel diseases, and a number of Accutane users have complained of these particular side effects. They are now among the most commonly cited side effects in Accutane lawsuits.

There are a growing number of Accutane users who believe that they were not adequately warned by the manufacturers of Accutane, Hoffman-La Roche, about the side effects associated with the medications, namely inflammatory bowel disease and other gastrointestinal problems. The Food and Drug Administration has acknowledged the risk of Accutane inflammatory bowel disease, and encouraged Hoffman-La Roche to list it as one of the possible side effects on Accutane packaging.

Accutane recall leaves some with questions

Hoffman-La Roche pulled Accutane from the United States’ pharmaceutical market in 2009 amid a number of lawsuits related to the drug. However, patients who were injured by Accutane are still eligible to file Accutane lawsuits as long as the statute of limitations in their state has not yet expired. Potential plaintiffs should contact an Accutane lawyer in order to establish whether or not they may be eligible to file suit against Hoffman-La Roche.

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Related Posts

  • Accutane Side Effects Lawsuits Award $ Millions
  • Accutane Lawsuits Continue
  • New Jersey Accutane Trial Still Pending

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