Accutane IBD Trial Underway

Many of the Accutane lawyers are not representing all that have suffered from this drug. This drug 13-cis retinoic acid is used many other drugs such as Renova 0.05% and 0.02% and was not labeled on the package containing this horrific molecule. The Transcript of 1990 on Accutane and Renova states that accutane isotretinoin was used in Renova and that they knew it caused vision problems, migraines, and irritable bowel syndrome and Crohns and birth defects. None of this was listed on Renova packaging. Only the patent stated it and now via the FOIA Act I received the NDA 19963 that clearly stated this. They knew this was a carcingenic and it should not be prescribed to melanoma patients and that was not listed. DMSO was involved in the chemistry and that is a known carcingenic. It causes irritable bowel syndrome and intestinal obstructions. Phosphorous is used in this chemistry and is listed as a poison with the Pharmacopeia as all agents used in Renova were listed and their toxicities from skin rashes, burns and blisters, migraines, dental carries, sinus problems, bone depletion, fractures of the bones, Keratitis, and blepharnephritis, severe abdominal pain, bloating, diarrhea and constipation that many of the chemicals used in combination with this chemo drug that was found to be too toxic for cancer patients, yet, dermatologist thought it was okay to prescribe to women and children and men for skin disorders. Tolene and cyclohexane and other gases used in these agents are toxic. Yet, no one is helping those of us who suffered severe adverse events from these agents. The Transcript of 1990 states that Johnson and Johnson and Hoffman and LaRoche depend on doctors reporting adverse events and that doctors are not doing their jobs. Had physicians done their jobs these toxic retinoid products would not have been approved on the market. The Pharmacopeia states these agents are not to be used on humans, yet they are being used on humans. Had the FDA and Johnson and Johnson reacted to my adverse event in 2000, which I had filed with both, Renova 0.02% wouldn't have been approved. Johnson and Johnson made a committment in having Renova approved that they would follow up on all future reactions this drug might have on humans. To date Johnson and Johnson has never seen me to investigate the horrific reactions I have endured. No one is telling the entire truth on how many injuries have been sustained by this toxic drug and how many products contained it that are not properly labeled. These drugs contain nuclea radioactive agents such as tritium and stated in the Transcript of 1990. This drugs are not being labeled radioactive violating the law on proper labeling.