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The FDA describes a facility where drug products intended to be sterile were produced in environments that may not have provided adequate contamination protection, where products that failed sterility and potency testing were released and distributed, where out-of-specification investigation procedures were not followed in a single documented case out of 23 reviewed, and where patients were not notified when the drugs they received were found to be subpotent or failed sterility testing
So I think its an interesting study, but (it) really portends us to really think about what our next steps are so we can get into more adjuvant approaches, in addition to this, at the same time, he added.
Childhood trauma predicts antidepressant response in adults with major depression: data from the randomized international study to predict optimized treatment for depression
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