Overview of pharmacovigilance practices at the largest academic healthcare system in the State of Qatar.
Moza Al HailWessam ElkassemAnas HamadPallivalappila AbdulroufBinny ThomasDerek StewartPublished in: International journal of clinical pharmacy (2018)
Adverse Drug Reactions (ADRs) are major global concern, adversely impacting patient safety and health outcomes. ADRs cause significant morbidity and mortality among hospitalised patients, causing greater length of hospital stay, increased healthcare costs and patient dissatisfaction to the treatments. Pharmacovigilance (PV), a process of detecting, monitoring and preventing drug-related harm, plays a vital role to ensure patient safety. ADR reporting is the cornerstone of PV. PV practices in Qatar are relatively new and are evolving rapidly. The purpose of this article is to explore the medication safety practices (notably ADR reporting) at the largest academic healthcare center in Qatar. The article further provides evidence on how information related to ADRs are generated and interpreted. Furthermore, it describes how a designated center for monitoring medication safety activities was established at the largest healthcare provider in Qatar.
Keyphrases
- adverse drug
- patient safety
- healthcare
- quality improvement
- primary care
- electronic health record
- drug induced
- end stage renal disease
- emergency department
- ejection fraction
- newly diagnosed
- chronic kidney disease
- health information
- case report
- peritoneal dialysis
- prognostic factors
- patient reported outcomes
- affordable care act
- social media