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Clinical Trial Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice

For example, if a weekly injection on Monday was missed, it could be given on Tuesday and then resume the normal schedule

Certain conditions are also responsible for depleting glycine levels

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These elements, which include fetal microchimerism, postpartum period, and female gender, are known to contribute a major part to the mechanism by which HT progresses