A Reflection of Educational Advancements In Undergraduate Medical Education From Pharmacological Perspective
Öz
Advances in technology accompanied by the rapid accumulation of new knowledge force higher education institutions to change the way in which they prepare their graduates for healthcare delivery systems. Medical education administrators in higher education should seek the appropiate curricular revisions that will yield the improvements in the lifelong academic performance of undergraduate medicine students. Adverse drug reactions and medical device incidents may cause “serious health issues” as shown in literature. There is no international standard exists for teaching pharmacovigilance at universities for undergraduate medical, pharmacy, dentistry, nursing and midwifery students. The aim of this review is to raise the awareness of the importance of pharmacovigilance, ecopharmacovigilance and medical device incidents in pharmacology curriculum in higher education and to underline the role of medical academics in encouraging undergraduate students for appropiate reporting of adverse drug reactions and medical device incidents to vigilance systems in accordance with national regulations and also in promoting for proper waste management and safe disposal of pharmaceuticals and personal care products.
Anahtar Kelimeler
Kaynakça
- 1.WHO. The Importance of Pharmacovigilance - Safety Monitoring of Medicinal Products, 2002; 1-52.
- 2.WHO. Pharmacovigilance: ensuring the safe use of medicines. WHO Policy Perspectives on Medicines, 2004; 1-5.
- 3.UMC, cited 12.03.2019, https://www.who-umc.org/about-us/our-story/
- 4.TMMDA, Turkish Medicines and Medical Devices Agency, Turkish Pharmacovigilance Center, cited 14.02.2019 https://www.titck.gov.tr/faaliyetalanlari/ilac/farmakovijilans.
- 5.Official Gazette. Regulation on the monitoring and assessment of the safety of medicinal products for human use, 2005, cited 12.03.2019 http://www.resmigazete.gov.tr/eskiler/2005/03/20050322-7.htm.
- 6.Ozcan G, Aykac E, Kasap Y, Nemutlu NT, Sen E, Aydinkarahaliloglu ND. Adverse Drug Reaction Reporting Pattern in Turkey: Analysis of the National Database in the Context of the First Pharmacovigilance Legislation. Drugs Real World Outcomes, 2016; 3(1):33–43.
- 7.Official Gazette. Regulatıon On The Safety Of Medıcınal Products By Turkish Medicines and Medical Devices Agency Legislation on Drug Safety, 2014; Official Gazette No: 28973 2014.
- 8.TMMDA Turkish Drug and Medical Device Agency. Guideline on Good Pharmacovigilance Practices: Module I - Management and reporting of adverse drug reactions Guideline on Good Pharmacovigilance Practices: Appendıx I – Definitions, 2014.
Ayrıntılar
Birincil Dil
İngilizce
Konular
Sağlık Kurumları Yönetimi
Bölüm
Derleme
Yazarlar
Evren Savlı
*
0000-0001-5052-5436
Türkiye
Evrim Savlı
Bu kişi benim
0000-0002-7158-0984
Türkiye
Yayımlanma Tarihi
30 Nisan 2019
Gönderilme Tarihi
8 Nisan 2019
Kabul Tarihi
11 Nisan 2019
Yayımlandığı Sayı
Yıl 2019 Cilt: 3 Sayı: 1