In the United States alone, the list of drugs classified as dangerous and causing more than two hundred thousand deaths each year continues to grow.
Clearly, the main reason these dangerous drugs cause such high mortality is the fact that some drug companies choose to produce drugs quickly to face many competitors. There are many things you have to face while inspection. You can know them in details and also search FDA 483 letters via various online sources.
The drug giants are philosophical that their scientists can continue to test their drugs while they are being mass produced, so as not to affect their marketing plans.
The results are often predictable. This amazing drug, which was launched just two weeks ago, is being pulled off the shelf because the Food and Drug Administration or drug companies themselves have discovered that it causes side effects that can cause permanent damage to your body. How this drug passes rigorous FDA research and testing is beyond rational thought.
The Food and Drug Administration must go through a rigorous review process before a seal of approval to place a new drug on the market is issued. If the review process is followed carefully, there is no need to withdraw drugs that are already on the market, right?
The problem, however, is that these drug companies sometimes find loopholes in FDA review results that the drug can be approved once minor changes are made by the drug company.
Sometimes at this point some evidence of serious side effects is pressed for FDA approval. It will not be withdrawn by the FDA until several complaints have been filed by users experiencing side effects after taking the drug.