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The Monte Carlo simulator could not be run at γ = 0.2, 95% excitation level due to a computational overflow problem.
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This assumes the drug can be characterized with direct acting pharmacodynamic models (absence of meaningful signal transduction delays) and that no tolerance develops or active metabolites are present
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This assumes the drug can be characterized with direct acting pharmacodynamic models (absence of meaningful signal transduction delays) and that no tolerance develops or active metabolites are present.
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