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Related Concept Videos

Prescription, Nonprescription and Orphan Drugs01:02

Prescription, Nonprescription and Orphan Drugs

Prescription drugs require a prescription from a medical practitioner and can only be obtained from a pharmacy. They have many applications, including treating pain, anxiety, and hypertension.
The misuse and addiction to prescription drugs is a growing problem that can affect people of all age groups, specifically teenagers. This can happen when prescription medications are used in ways not intended by the prescriber, such as taking someone else's prescription or using medication for...
Pharmaceutical Poisoning: Potential Scenarios01:26

Pharmaceutical Poisoning: Potential Scenarios

Pharmaceutical poisoning can occur through various channels, impacting an estimated 2 million hospitalized patients in the U.S. annually with serious adverse drug responses. These scenarios encompass both therapeutic uses, such as drug toxicity, where even standard dosages can lead to severe central nervous system depression, and non-therapeutic exposures, including accidental ingestion by children, and environmental and occupational exposures.Unintentional poisonings often involve exploratory...
Drug Control Governance: Regulatory Bodies and Their Impact01:03

Drug Control Governance: Regulatory Bodies and Their Impact

Drug control governance involves the oversight and regulation of pharmaceuticals to ensure their safety and efficacy while preventing illegal drug use and trafficking. Regulatory bodies, including the US Food and Drug Administration (FDA) and the European Union's European Medicines Agency (EMA), play a central role in this process. These agencies evaluate the safety and efficacy of drugs before they can be marketed. They fund clinical trials and assess the benefits and risks associated with a...
Drug Classes and Categories01:25

Drug Classes and Categories

Drugs can be classified according to their chemical composition or their intended therapeutic application. For instance, anti-infective agents that possess the ability to eliminate pathogens or suppress their growth and reproduction can be grouped based on the organisms they target or their chemical structure. Furthermore, drugs can be divided into prescription, nonprescription, or controlled substances. Prescription medications, such as antibiotics, require oversight from a licensed healthcare...
Dose-Response Relationship: Selectivity and Specificity01:25

Dose-Response Relationship: Selectivity and Specificity

Drugs exert their therapeutic effects by interacting with receptors, enzymes, or ion channels that are present throughout the human body. The strength and duration of the interaction between a drug and its target receptor are characterized by the selectivity and specificity of the drug. Selectivity refers to a drug's strong preference for its intended target over other targets. For instance, isoprenaline, a non-selective β-adrenergic agonist, interacts with both β1- and β2-adrenergic receptors...
Pharmaceutical Alternatives: Excipients and Impurities-Related Therapeutic Nonequivalence01:19

Pharmaceutical Alternatives: Excipients and Impurities-Related Therapeutic Nonequivalence

Pharmaceutical products contain more than just the active drug; they also contain various excipients such as binders, solubilizers, stabilizers, preservatives, and other elements. In some cases, impurities or contaminants might be present. Traditionally, quality control in pharmaceuticals has primarily focused on the analysis of the active drug, often overlooking the impact of these additional components. The recent issue with heparin contamination by over-sulfated chondroitin sulfate, a...

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Multiplex Therapeutic Drug Monitoring by Isotope-dilution HPLC-MS/MS of Antibiotics in Critical Illnesses
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Can the selection and use of essential medicines decrease inappropriate drug use?

M M Reidenberg1

  • 1Department of Pharmacology, Weill Cornell Medical College, New York, New York, USA. mmreid@med.cornell.edu

Clinical Pharmacology and Therapeutics
|May 20, 2009
PubMed
Summary
This summary is machine-generated.

The World Health Organization (WHO) estimates half of all medicines are misused. Implementing an essential medicines list can improve prescribing practices and reduce inappropriate drug use globally.

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Area of Science:

  • Pharmacoeconomics
  • Public Health Policy
  • Drug Utilization

Background:

  • The World Health Organization (WHO) reports that approximately 50% of medicines are inappropriately prescribed, dispensed, sold, or consumed.
  • Suboptimal medication use leads to increased healthcare costs and adverse health outcomes.

Purpose of the Study:

  • To evaluate the impact of utilizing an essential medicines list on prescribing practices.
  • To advocate for a comprehensive approach to reduce inappropriate drug use.

Main Methods:

  • Analysis of prescribing patterns and drug utilization.
  • Review of administrative strategies to manage drug lists.

Main Results:

  • Selection from a curated list of essential medicines can decrease inappropriate prescribing by limiting the use of less effective or more toxic alternatives.
  • Prescribers gain a deeper understanding of a smaller formulary, potentially improving medication safety.

Conclusions:

  • Implementing the essential medicines concept is a viable strategy to decrease inappropriate drug use.
  • Overcoming limitations such as restricted prescribing of unlisted drugs and delays in updating the list requires administrative action.
  • A global, committed approach is necessary to effectively eliminate inappropriate medication practices.