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Related Concept Videos

Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
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...
Therapeutic Drug Monitoring: Affecting Factors01:29

Therapeutic Drug Monitoring: Affecting Factors

Therapeutic Drug Monitoring (TDM) is the clinical practice of measuring specific drug levels in a patient's blood or body tissues to manage and optimize therapy. TDM is crucial for drugs with narrow therapeutic windows, like warfarin and phenytoin, where incorrect doses can lead to treatment failure or severe side effects. This monitoring ensures the dosage administered is within a safe and effective range. The factors affecting therapeutic drug monitoring include:Patient-Specific Factors:a.
Therapeutic Drug Monitoring: Drug Analysis Methods01:26

Therapeutic Drug Monitoring: Drug Analysis Methods

Therapeutic Drug Monitoring (TDM) is a clinical practice that measures specific drug levels in a patient's blood or body tissues to tailor drug therapy effectively. This monitoring is critical for managing drugs with narrow therapeutic indices like digoxin and phenytoin, ensuring they are both safe and effective. For instance, monitoring theophylline levels in asthma patients involves precision and sensitivity to adjust doses according to individual responses to therapy, ensuring efficacy and...
Errors occurring during blood pressure monitoring01:25

Errors occurring during blood pressure monitoring

Blood pressure monitoring is a crucial clinical procedure in diagnosing and managing various cardiovascular conditions. Despite its significance, the accuracy of blood pressure measurements can be compromised by multiple factors, potentially leading to either falsely high or low readings. These inaccuracies are critical as they can significantly impact patient care. So, it is vital to understand these challenges deeply and adopt strategic approaches to minimize errors.
Several factors...
Therapeutic Drug Monitoring: Overview and Classification01:16

Therapeutic Drug Monitoring: Overview and Classification

Therapeutic Drug Monitoring (TDM) is a clinical practice that measures specific drug levels in a patient's blood at designated intervals to ensure the drug concentration stays within a therapeutic range. This monitoring is crucial for optimizing individual dosage regimens, enhancing therapeutic efficacy, and minimizing drug-related toxicity. TDM is vital for drugs with narrow therapeutic windows, significant variability in pharmacokinetics, and a clear correlation between plasma levels and...

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Updated: May 13, 2026

Multiplex Therapeutic Drug Monitoring by Isotope-dilution HPLC-MS/MS of Antibiotics in Critical Illnesses
11:17

Multiplex Therapeutic Drug Monitoring by Isotope-dilution HPLC-MS/MS of Antibiotics in Critical Illnesses

Published on: August 30, 2018

Medication errors through a national pharmacovigilance database approach: a study for Malta.

Amy Tanti1, Miriam Camilleri, Patricia Vella Bonanno

  • 1Medicines Authority, 203 Level 3, Rue D'Argens, Gzira, GZR, Malta.

The International Journal of Risk & Safety in Medicine
|February 28, 2013
PubMed
Summary

Medication errors in Malta, particularly with NSAIDs and antibiotics, were identified through pharmacovigilance data. Most errors occurred in the community during prescribing and monitoring stages, some causing serious harm.

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Area of Science:

  • Pharmacovigilance and Drug Safety
  • Medication Error Analysis
  • Public Health

Background:

  • Medication errors pose a significant risk to patient safety.
  • Understanding the patterns of medication errors is crucial for developing targeted interventions.
  • The Maltese pharmacovigilance database offers a valuable resource for identifying and analyzing these events.

Purpose of the Study:

  • To identify and characterize medication errors reported in the Maltese pharmacovigilance database.
  • To determine the frequency and types of medication errors.
  • To describe the stages of medication use where errors occur and associated drug classes.

Main Methods:

  • Retrospective analysis of Adverse Drug Events (ADEs) reported over a 5-year period in Malta.
  • Identification of medication errors by comparing drug use against the Summary of Product Characteristics (SmPC).
  • Classification of errors by type, seriousness, and stage within the medication use chain.

Main Results:

  • 319 ADE reports met the inclusion criteria; 56 were associated with serious patient harm.
  • The 50-59 and 80-89 age groups were most frequently associated with medication errors.
  • 65% of errors originated in the community, primarily during prescribing (52%) and therapeutic monitoring (26%).
  • Non-steroidal anti-inflammatory drugs (NSAIDs) and antibiotics were commonly involved in errors related to dosage, monitoring, interactions, and duration.

Conclusions:

  • Pharmacovigilance databases are effective tools for detecting medication errors.
  • The findings highlight specific areas and drug classes requiring attention to reduce medication-related harm.
  • This study underscores the utility of pharmacovigilance data in enhancing medicinal product safety.