Actos (Pioglitazone HCl) which is marketed as Actos, Actoplus Met®, and Duetact®, was reported to be linked to an increased incidence of BLADDER CANCER according to the FDA Safety announcement of September 17th.
While the ten year study did not show an absolute link between all taking Actos and bladder cancer, an increased risk of bladder cancer was observed among patients with the longest exposure to Actos, as well as in those exposed to the highest cumulative dose of Actos.
If you believe you have been affected by Actos and you need assistance with filing an actos lawsuit or want to be involved in any possible settlement, you can speak with someone now who is experienced with the tragedy of drugs that harmed when they were meant to heal.
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Over the past few years, Zoloft has been linked to patient reports of increased depression and suicidal behavior, the number of zoloft lawsuits has skyrocketed over the past few years. Several drug advisory committees including the Food and Drug Administration (FDA) and the Psychopharmacological Drugs Advisory Committee (PDAC) continue to investigate these claims.
Pfizer began marketing the Zoloft in 1992. Today, Zoloft generates $2 billion dollars in annual sales and is among Pfizer’s top selling drugs. It is prescribed to both adult and pediatric patients and marketed as a versatile drug that can treat six mood and anxiety disorders, psychiatric and non-psychiatric disorders.
Since the early 1990s numerous world class experts have warned about the role of SSRI-induced akathisia in violence and suicide. On March 19, 1996, the FDA wrote to Pfizer stating: “We note that there appears to be an increased frequency of reports of suicidality in the pediatric/adolescent patients exposed to Sertraline [Zoloft] compared to either placebo or Sertraline-treated OCD patients. If this is in fact the case what would be a plausible explanation?” Birth Defect Lawsuit Zoloft.
