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A Patient's Right to Choose

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Submitted By rmkdak
Words 1789
Pages 8
Running head: PATIENT’S RIGHT

A Patient's Right to Choose
Abstract
The U. S. Food and Drug Administration must expand access to experimental, unapproved drugs to include terminally-ill patients who have exhausted all conventional treatment methods and choose to accept the risks. Terminally-ill patients deserve the right to choose and have access to potentially life-saving drugs as the potential benefit of life justifies the potential risks when imminent death is their only alternative. After extensive testing many of these drugs go on to be approved, but this process can take years and often terminally-ill patients die long before FDA approval. By allowing dying patients the choice of participation in clinical trials, not only could life be spared, but the possible proven efficacy of these drugs could be of benefit to all humanity. A Patient's Right to Choose
It is the constitutional right of the citizens of the United States of America to make an informed decision as to whether or not to use potentially life-saving drugs to prolong life when terminally ill. Federal regulations and restrictions must be lifted to accommodate access to this fundamental right. When faced with a terminal illness and all conventional treatment methods have failed, it should be the patient's choice as to whether or not unapproved, experimental drugs are used, as the potential benefit of life justifies the potential risks when imminent death is the alternative with no other options.
Drug Approval Process
The U. S. Food and Drug Administration’s Center for Drug Evaluation and Research (CDER) currently evaluates and dictates when new drugs can be prescribed and dispensed to the public. According to the Food and Drug Administration (2009), when pharmaceutical drug companies want to market a new drug, it must first be tested and supporting evidence must be submitted proving it is

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