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submitted by: admin on 11/21/2024
The karma of Big Pharma is revealed in a discussion of the business orientation and lack of ethics. Direct to consumer ads are banned in all countries except the US and New Zealand. Big pharma spends billions every year on DTC ads. Profit is the purpose. More money is spent on advertizing that on research! We are clearly susceptible to DTC ads, they sell prescription...
submitted by: admin on 11/21/2024
The karma of Big Pharma is revealed in a discussion of the business orientation and lack of ethics. Direct to consumer ads are banned in all countries except the US and New Zealand. Big pharma spends billions every year on DTC ads. Profit is the purpose. More money is spent on advertizing that on research! We are clearly susceptible to DTC ads, they sell prescription...
submitted by: admin on 09/20/2013
The scandalous swine flu vaccine is still being promoted by the CDC when it is clear that the vaccine is unproven to be of value, may not be safe, may increase the risk for getting the flu, and that its seriousness is no worse than the common cold. Nonetheless, two counties and many hospitals in northern California are mandated that health care professionals...
submitted by: admin on 06/02/2020
submitted by: admin on 10/18/2014
Dr. Len and nurse Vicki break down the real facts about Ebola in this 20 minute radio show!
Why has Ebola attracted international attention that is freaking out millions of people around the world? Is there an actual pandemic? True enough that there have been more deaths this year than combined since 1976, and that has people worried. However,...
submitted by: admin on 09/20/2013
Drug reps know how to sway doctors to use the drugs their company makes using a variety of social techniques. The accuracy and legality of how they operate is discussed. Off-label usage is reviewed.
submitted by: admin on 09/21/2013
Tens of thousands of metal on metal artificial hips are failing years earlier than expected and are requiring a second surgery to take the old device out and put in a new one. There has been no tracking system to follow how they do, although after the fact a tracking system is being implemented by orthopedists now. This is coming at a price of about $1 billion....
submitted by: admin on 11/21/2024
Certain drugs should be made available as soon as possible. However, generally this approach leads to a conflict of interest between the FDA and Big Pharma that brings drugs to market much easier.
submitted by: admin on 09/21/2013
The FDA and USDA are not protecting our food supply. Melamine, lead, mercury, and diethylene glycol are examples of what can get into our food supply. The melamine and diethylene glycol stories are discussed.
submitted by: admin on 09/21/2013
The FDA is considering offering many prescription drugs without a prescription at pharmacies where a few questions would be asked and medicine dispensed like through a vending machine! Most insurances would not be required to pay for such costs and patients would be largely on their own to determine the need and safety of their purchases.
While...
submitted by: admin on 09/21/2013
When you have a side effect from a medication you can report it to the FDA yourself; MDs have a history of not reporting side effects to the FDA They are simply too busy. This is especially problematic when patients are on a multitude of drugs; which one caused the problem? The example of side effects from statins is described. The number to call is 1-800-FDA-1088.
submitted by: admin on 09/21/2013
The FDA is considering allowing more drugs to become over-the-counter as their patents run out. This, of course, would make it possible for Big Pharma to make greater profits. However, there are serious challenges related to safety in using drugs such as statins and drugs for type 2 diabetes that would emerge. Most people are not sufficiently educated...
submitted by: admin on 09/21/2013
After 50 years the FDA is pulling Darvon off the market. What took so long and what does it reflect in terms of how the FDA works and how Big Pharma withholds what it knows about the side effects of its drugs. Thousands of people have died from heart rhythm disturbances. The lack of ethics, the conflicts of interest, and the dishonesty of the pharmaceutical industry...
submitted by: admin on 11/21/2024
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submitted by: admin on 04/12/2015
The FDA is recommending that physicians restrict prescribing high-dose Zocor because of an increased risk of muscle damage that can lead to pain and also the release of large amounts of myoglobin from muscle from a process called rhabdomyolysis, which can lead to renal failure and death. They also warned that the use of several anti-fungal agents such as Sporonox,...
submitted by: admin on 11/21/2024
Even though Avandia increases both heart attacks and heart deaths the FDA has been lax in dealing with this problem. The incestuous relationship between the FDA and Big Pharma is disclosed.
submitted by: admin on 11/21/2024
Should supplements be regulated by a competent FDA is a legitamate question. There are too many false claims on supplements and regulation is limited by the FDA. There is also a political aspect involving Big Pharma, physicians, and the supplement industry that gets heated. There are about 10,000 hospitalizations caused by use of supplements, but millions from...
submitted by: admin on 09/21/2013
The FDA is requiring that Avodart and Proscar manufacturers disclose that there is an approximately 50% increased incidence of high grade prostate cancer with their usage. It also pointed out that they are not approved for prostate cancer prevention. These drugs block the conversion of testosterone to dihydro-testosterone, which is believed to be one the causes...
submitted by: admin on 01/17/2015
The FDA has officially linked all statins with cognitive problems like forgetfullness and confusion as well as with a 25% increased risk for an elevated blood sugar level and possible association with type 2 diabetes. Statins are the best selling drugs on the market and are used by 21 million people in the US each year. Of course, there are all the other side...
submitted by: admin on 09/21/2013
Can we trust the FDA to protect us from Big Pharma and from the supplement industry? Fast tracking drugs has plusses and minuses. Should patients have the choice of trying drugs that are not yet on the market? Can we trust the drugs that are on the market that don't do that much? How much do conflicts of interest come into play?