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Precision dosing to avoid adverse drug reactions

机译:精密剂量以避免不良药物反应

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Adverse drug reactions (ADRs) have traditionally been managed by trial and error, adjusting drug and dose selection reactively following patient harm. With an improved understanding of ADRs, and the patient characteristics that increase susceptibility, precision medicine technologies enable a proactive approach to ADRs and support clinicians to change prescribing accordingly. This commentary revisits the famous pharmacology–toxicology continuum first postulated by Paracelsus 500?years ago and explains why precision dosing is needed to help avoid ADRs in modern clinical practice. Strategies on how to improve precision dosing are given, including more research to establish better precision dosing targets in the cases of greatest need, easier access to dosing instructions via e-prescribing, improved monitoring of patients with novel biomarkers of drug response, and further application of model-informed precision dosing.
机译:不良药物反应(ADRS)传统上通过试验和误差来管理,调整药物和剂量选择,随后患者伤害。随着对ADR的了解,提高了易感性的患者特征,精密医学技术能够积极主动地接近ADR和支持临床医生,以相应地改变处方。该评论重新评估着名的药理学毒理学毒理学毒理学毒理学首先由Paracelsus 500发表于帕拉克斯500岁?几年前,并解释了为什么需要精确给药来帮助避免现代临床实践中的ADR。给出了如何提高精密剂量的策略,包括更多研究,在最大的需求中建立更好的精确剂量目标,更容易通过电子处方能够进行给药指令,改善了对药物反应的新型生物标志物的患者的监测,以及进一步的应用模型明智的精密剂量。

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