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Does anyone out there know how to find out how the FDA evaluated a medicine before one actually ingests it? I am aware of the package inserts, but would like to know on what information the decision that the medicine is "safe" is based.
I no longer trust that any new drug is safe, just because companies are allowed to sell it. At the same time, I don't want to automatically disregard all new medicines because there have been some problems in the past.
How do others with serious illnesses deal with this issue?
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