Executive Summary Humira is taken for autoimmune disorders. What was never done with Humira’s FDA approval was to evaluate any cost-benefit for this drug. Introduction Humira has significant side effects for improvement against autoimmune diseases. It also comes high costs and exaggerated benefits. This article will begin by discussing its financial costs and then move…
Executive Summary Humira is taken for autoimmune disorders. Investigating Humira brings up the topic of whether this is a sustainable solution. Introduction Ivermectin is a very important immunomodulator. However, it is very rare to hear about Ivermectin for autoimmune disorders. However, we received a question on just this topic. As the person posing the question…
Executive Summary We received a question on the use of Ivermectin for Crohn’s disease. Introduction Ivermectin is a very important immunomodulator. However, it is very rare to hear about Ivermectin for autoimmune disorders. However, we received a question on just this topic. Wait One Second… Why is The Article Not Viewable? You are seeing this…
Executive Summary The US pharmaceutical policies result in the highest drug prices in the world. Canada has much more reasonable drug prices. Introduction Canada’s drug regulation is far more effective in managing drug prices than the US. Wait One Second… Why is The Article Not Viewable? You are seeing this text instead of the article…
Executive Summary Generics were proposed to decrease the cost of drugs in the US greatly. Why did this outcome not occur as predicted? Introduction One of the most widely accepted assumptions is that generic drugs reduce the cost of drugs in the US. We cover in this article why this assumption, while perfectly rational, is…
Executive Summary The FDA has a long history of covering up clinical trial fraud by pharmaceutical companies. Introduction The less one knows about the FDA, the more legitimate the agency appears, and conversely, the more one looks into the behavior of the FDA, the worse the story gets. Wait One Second… Why is The Article…
Executive Summary Falsifying bioequivalence tests for approval are done frequently — and the FDA does not do anything about false bioequivalence when pointed directly to it. Introduction The FDA promotes bioequivalence as the case with all generics, even those made in India that fail their inspections, often have their bioequivalence trials falsified. Wait One Second……
Executive Summary Side effects of chemotherapy are usually listed in an antiseptic way at the major medical sites that promote chemotherapy. The following are first-hand accounts of the side effects. Introduction The side effects of chemotherapy are horrid. And it is essential to do what oncologists and cancer centers don’t want patients to do —…
Executive Summary Falsifying bioequivalence is commonly done by what is called clinical research organizations or CROs. Introduction A significant issue with falsifying bioequivalence is the companies paid to prove rather than test bioequivalence. These are called Clinical Research Organizations or CROs. Wait One Second… Why is The Article Not Viewable? You are seeing this text…
Executive Summary Bioequivalence testing is much more complicated and fraught with limitations than generally understood. The World Health Organization and Generic Drug Production Introduction Patients are repeatedly told there is no difference between generics and brand-name drugs. How this assertion is proven tends to be left out of the conversation, and that is what we…