
The individualization of drug dosage to maximize benefit and minimize risk is always a challenge since desired benefit is often associated with many dose‐related adverse effects. Most disease is subacute and mild to moderate in severity. Doses that give around 50% of the maximum possible drug effect [the effective dose 50 (ED50)] often prove to be sufficient. An analysis of the dose–response relationship for most drugs shows that above the ED50, efficacy increases only marginally, whilst adverse effects continue to increase (Figure 1), especially with agonist agents. Using the lowest effective dosage is particularly desirable when drugs are used long term in prevention, as is the case with most cardiovascular drugs. Open in a separate window Figure 1 A graphical representation showing relationship of drug dose and effect – toxicity and clinical
pharmaceutical marketing, Clinical Trials as Topic, Dose-Response Relationship, Drug, Evidence-Based Practice, Humans, dose–response, effective dose 50
pharmaceutical marketing, Clinical Trials as Topic, Dose-Response Relationship, Drug, Evidence-Based Practice, Humans, dose–response, effective dose 50
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 37 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
