2020
DOI: 10.3389/fphar.2020.00420
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Precision Dosing Priority Criteria: Drug, Disease, and Patient Population Variables

Abstract: The administered dose of a drug modulates whether patients will experience optimal effectiveness, toxicity including death, or no effect at all. Dosing is particularly important for diseases and/or drugs where the drug can decrease severe morbidity or prolong life. Likewise, dosing is important where the drug can cause death or severe morbidity. Since we believe there are many examples where more precise dosing could benefit patients, it is worthwhile to consider how to prioritize drug-disease targets. One key… Show more

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Cited by 64 publications
(58 citation statements)
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References 144 publications
(164 reference statements)
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“…We also note that many computational repurposing predictions are mechanistic or statistical only, and will require separate evaluation for specific medical indications and patient populations. It is well known, for instance, that drug metabolism and pharmacodynamics are influenced by gender, age, concomitant medications and food intake, as well as underlying physiological states, and thus drug repurposing from one indication to another still necessitates a thorough understanding of the individual and disease-specific clinical safety parameters [129,130]. FDA maintains both the 'passive' postmarketing pharmacovigilance database FAERS (FDA Adverse Event Reporting System) and the 'active' sentinel system, which collect information on adverse events that may occur in patients outside the clinical trials in the long term.…”
Section: Expert Opinionmentioning
confidence: 99%
“…We also note that many computational repurposing predictions are mechanistic or statistical only, and will require separate evaluation for specific medical indications and patient populations. It is well known, for instance, that drug metabolism and pharmacodynamics are influenced by gender, age, concomitant medications and food intake, as well as underlying physiological states, and thus drug repurposing from one indication to another still necessitates a thorough understanding of the individual and disease-specific clinical safety parameters [129,130]. FDA maintains both the 'passive' postmarketing pharmacovigilance database FAERS (FDA Adverse Event Reporting System) and the 'active' sentinel system, which collect information on adverse events that may occur in patients outside the clinical trials in the long term.…”
Section: Expert Opinionmentioning
confidence: 99%
“…3D printing allows for tailoring of dosage forms to patients' and disease needs such as age, dose, release profile, colour, texture, taste, and size [5]. Their ability to allow for dose individualisation enables 3D printed dosage forms to ensure efficacy combined with minimal side effects [6]. 3D printing makes feasible the incorporation of multiple active pharmaceutical ingredients (API) into one dosage form that can result in enhanced adherence and better and safer pharmacotherapy in polymedicated patients [7].…”
Section: Introductionmentioning
confidence: 99%
“…With the prospect of novel digital health care devices (e.g., point‐of‐care devices), more frequent monitoring could become clinical reality. Real‐world data is currently underutilized 51 but has great potential to improve MIPD, as shown in this study. The current approach is limited to misspecifications or population shifts on the structural model parameter level.…”
Section: Discussionmentioning
confidence: 89%