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Does it Really Matter What the FDA Says at This Point?

My brother sent me an interesting article about a drug called Qnexa that is about to come on the market.   The company that makes it, Vivus Inc, claims that Qnexa, which combines the appetite suppressant phentermine and anti-seizure drug topiramate, helped patients lose at least 10 percent of their weight after a year of treatment.

You can read the rest of the article here: U.S. Advisers Back Experimental Obesity Pill

So here is what I have to say about this…..

If you read the article, it is basically discussing the fact that this drug has already been rejected by the FDA two years ago, but a panel of outside experts called the “US health advisors” (whoever these people are and represent) recommend approving the drug despite the many potential side effects such as heart attacks and birth defects, because there are just too many obese people and something needs to be done about it.

So, if the FDA does what it is usually does and follows the recommendations of this panel – the “US Health Advisors” (whoever these people are and represent)…this drug will be available sometime in April.

Who cares what the FDA approves and what they don’t approve anymore?  They have approved drugs that have killed many people and will continue to approve many, many more dangerous drugs…..why not approve a drug like this one?

What difference does it make?

Slap a label on the bottle listing all the possible side effects (like death) and leave it up to those who decide that it is worth the risk.

At some point, we, Americans, have to take responsibility for ourselves and our own lives and forget about what the FDA “approves” of and what they don’t “approve” of.

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