The US Food and Drug Administration (FDA) has approved a new cancer drug that allegedly treats the deadly side effects caused by another popular cancer drug. The new drug, Voraxaze (glucarpidase), is said to expel methotrexate, a commonly prescribed and highly toxic chemotherapy drug, from the body. But Voraxaze comes with its own set of harmful side effects, which shows that approving drugs to treat the side effects of other drugs is an endless, but highly profitable, cycle of toxicity.
Methotrexate's known side effects include kidney and liver destruction, skin rashes, mouth sores, damaged intestines, and death. The drug often lingers in the body following cancer treatments, as weakened organs become increasingly incapable of expelling it from the body. So to "fix" this problem, the FDA has decided to approve another drug that it says breaks down methotrexate and eliminates it from the system.
But Voraxaze, which is made from genetically-modified (GM) enzymes, carries with it harmful side effects of its own, including hypertension, arrhythmia, allergic dermatitis, nausea, and vomiting. And these are just the short-term side effects observed among a small clinical trial group of just 290 patients, which is the only trial that has been conducted evaluating the safety of Voraxaze.
Worse, Voraxaze received "fast-track" approval from the FDA based on a single clinical study of just 22 patients, which allegedly evaluated the drug's effectiveness. By all reasonable scientific standards, a single study with this ridiculously small amount of participants can hardly be considered a valid indicator of a drug's efficacy (http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm287997.htm).
Contrast this with mainstream medicine's rejection of at least 24 separate studies, all with much larger sample sizes, that have identified a clear and definitive link between fluoride consumption and disease in recent days. "Further research" is always necessary when the issue involves proving fluoride's toxicity, or proving the benefits of an herbal or dietary supplement. But when a new drug is up for approval, one small, industry-funded study is enough for regulators.
So thousands of cancer patients who become poisoned by methotrexate, which is also used to treat psoriasis and arthritis patients, will also now receive an intravenous dose of GM enzymes that have never been definitively proven either safe or effective. Leave it to the FDA to once again pander to Big Pharma at the expense of public health.
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