Drug-induced diseases: approaches to diagnosis, correction and prevention. Pharmacovigilance


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Abstract

Drug-induced diseases (DIDs) are a variant of undesirable drug reactions that can increase mortality and/or morbidity and/or cause symptoms that force the patient to seek medical attention or lead to hospitalization. There are certain approaches to the management of patients that can improve the efficiency of diagnosis and prevention of DIDs. One of the key moments is accuracy in the pharmacological history taking. The pharmacological history should be accumulated from various sources: from the patient, relatives or guardian, caregiver; inspection of containers with medicines (drugs), blisters, packaging of drugs; various medical documents (extracts, conclusions of consultations of specialists, results of laboratory and instrumental studies), etc. Information in the medical history should include patient’s demographic data, social habits, allergic history; detailed information should be collected about all prescription and over-the-counter drugs taken by the patient during the previous 6 months, including those that he is no longer taking at the moment. A mandatory assessment of laboratory test data is also required. The main task in the diagnosis and differential diagnosis of DIDs is to determine the possible causal relationship between taking the drug and the development of an undesirable side reaction. For these purposes, special scales and algorithms are used, for example, the Naranjo algorithm. The main principle of the correction of DIDs is the cancellation of the inducer drug or its replacement with another drug that does not have such side effects. The training of patients, the timely detection of adverse drug reactions by medical personnel and the spontaneous reporting of their development to the relevant executive authorities (pharmacovigilance) as required by law are critical for the prevention of the development of DIDs in the future.

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About the authors

D. A Sychev

Russian Medical Academy of Continuous Professional Education, Department of Clinical Pharmacology and Therapy

Olga D. Ostroumova

Russian Medical Academy of Continuous Professional Education; I.M. Sechenov First Moscow State Medical University (Sechenov University)

Email: ostroumova.olga@mail.ru
Dr. Sci. (Med.), Professor, Head of the Department of Therapy and Polymorbid Pathology

A. P Pereverzev

Russian Medical Academy of Continuous Professional Education

A. I Kochetkov

Russian Medical Academy of Continuous Professional Education

T. M Ostroumova

I.M. Sechenov First Moscow State Medical University (Sechenov University)

M. V Klepikova

Russian Medical Academy of Continuous Professional Education

I. A Alyautdinova

Russian Medical Academy of Continuous Professional Education

I. V Goloborodova

A.I. Yevdokimov Moscow State University of Medicine and Dentistry

References

  1. Tisdale J.E., Miller D.A. Drug Induced Diseases: Prevention, Detection, and Management. 3rd Ed. Bethesda, Md.: American Society of Health-System Pharmacists; 2018. 1399 р
  2. Сычев Д.А. (ред.). Полипрагмазия в клинической практике: проблема и решения (учебное пособие). 2-е изд., испр. и доп. СПб.: ЦОП «Профессия», 2018. 272 с
  3. Bouvy J.C., De Bruin M.L., Koopmanschap M.A. Epidemiology of Adverse Drug Reactions in Europe: A Review of Recent Observational Studies. Drug Saf 2015;38(5):437-53. doi: 10.1007/s40264-015-0281-0
  4. Lea M, Mowe M., Mathiesen L., et al. Prevalence and risk factors of drug-related hospitalizations in multimorbid patients admitted to an internal medicine ward. PLoS ONE. 2019;14(7):e0220071. Doi: https://doi.org/10.1371/journal. pone.0220071
  5. Tandon V.R., Khajuria V, Mahajan V, et al. Drug-induced diseases (DIDs): An experience of a tertiary care teaching hospital from India. Indian J Med Res. 2015;142(1):33-9. doi: 10.4103/09715916.162093
  6. Meier F, Maas R., Sonst A., et al. Adverse drug events in patients admitted to an emergency department: an analysis of direct costs. Pharmacoepidemiol Drug Saf. 2015;24(2):176 86. doi: 10.1002/pds.3663
  7. Reeder T.A., Mutnick A. Pharmacist-versus Physician-obtained medication histories. Am J Health-Syst Pharm. 2008;65(9):857-60. doi: 10.2146/ajhp070292
  8. URL: www.euro.who.int/ru/health-topics/ disease-prevention/alcohol-use/do-you-drink-too-much-test-your-own-alcohol-consumption-with-the-audit-test/take-the-audit-test-now. Дата обращения/date of access 17.04.2020
  9. Петров Д.В. Диагностика, лечение и профилактика расстройств, вызванных употреблением алкоголя. Ярославль, 2003. С. 90-2
  10. Первичная профилактика психических, неврологических и психосоциальных расстройств. М.: Смысл, 2002. С. 126-27
  11. The Uppsals Monitoring Centre. The Use of the WHO-UMC System for Standardised Case Causality Assessment. https://www.who-ums. org/media/2768/standartised-case-causality-assessment.pdf (дата обращения/date of access 17.04.2020)
  12. Naranjo C.A., Busto U., Sellers E.M., et al. A metod for estimating the probability of adverse drug reactions. Clin Pharmacol Ther. 1981;30(2):239 45. doi: 10.1038/clpt.1981.154
  13. US Food and Drug Administration. MedWatch: the FDA safety information and adverse event program. http:/www. fda.gov/safety/medwatch (accessed 2020 Arp 17)
  14. Федеральный закон (ред. от 03.04.2020) «Об обращении лекарственных средств» № 61-ФЗ от 12.04.2010. Ст. 64. Фармаконадзор (в ред. Федерального закона № 429-ФЗ от 22.12.2014)
  15. Приказ Росздравнадзора «Об утверждении порядка осуществления фармаконадзора» № 1071 от 15.02.2017. [Order of Roszdravnadzor "On approval of the procedure for pharmacovigilance" No. 1071 dated 02.15.2017. (In Russ.)]. URL: https://roszdravnadzor.ru/i/upload/imag es/2017/3/23/1490263188.17346-1-14369. pdf. Дата обращения/date of access 17.04.2020
  16. Официальный сайт Всемирной организации здравоохранения. [The official website of the World Health Organization. (In Russ.)]. URL: https://www.who.int/ (дата обращения/date of access: 17.04.2020)
  17. Официальный сайт сотрудничающего центра ВОЗ по мониторингу нежелательных реакций, расположенного в городе Уппсала, Швеция (WHO-UMC). [Official site of the WHO collaborating center for monitoring adverse reactions, located in Uppsala, Sweden (WHO- UMC). (In Russ.)]. URL: https://www.who-umc. org. Дата обращения/date of access: 17.04.2020.
  18. Официальный сайт базы данных нежелательных реакций ВОЗ VigiBase. [Official website of the WHO VigiBase adverse reaction database. (In Russ.)]. URL: http://www.vigiaccess.org. Дата обращения/date of access 17.04.2020.
  19. Решение Совета Евразийской экономической комиссии «Об утверждении Правил надлежащей практики фармаконадзора Евразийского экономического союза» № 87 от 03.11.2016. [Decision of the Council of the Eurasian Economic Commission "On approval of the Rules of Good Practice for Pharmacovigilance of the Eurasian Economic Union" No. 87 dated 03.11.2016. (In Russ.)]. URL: http://www.eurasiancommission. org. Дата обращения/date of access 17.04.2020.
  20. Федеральный закон «Об обращении лекарственных средств» № 61-ФЗ от 12.04.2010 (в ред. Федерального закона № 105-ФЗ от 03.04.2020). [Federal Law «On the Circulation of Medicines» No. 61-ФЗ dated 04/12/2010 (as amended by Federal Law No. 105-ФЗ dated 04/03/2020). (In Russ.)].
  21. Астахова А.В., Лепахин В.К. Лекарства. Неблагоприятные побочные реакции и контроль безопасности. 2-е изд., испр. и доп. М.: Эксмо, 2008. 256 с. (Профессиональная медицина). [AstakhovaA.V, Lepakhin VK. Medication. Adverse Adverse Reactions and Safety Monitoring. 2nd ed., Rev. and add. M.: Eksmo, 2008. 256 p. (Professionalmedicine). (In Russ.)].
  22. Официальный сайт Агентства по контролю за пищевыми продуктами и лекарственными средствами США. [U.S. Food and Drug Administration Official Website. (In Russ.)]. URL: https:// www.fda.gov. Дата обращения/date of access 17.04.2020.
  23. Официальный сайт Агентства по контролю лекарственных средств и продуктов, используемых в здравоохранении (Medicines and Healthcare products Regulatory Agency). URL: https://www.gov.uk. Дата обращения/date of access 17.04.2020.
  24. Меркулов В.А., Бунятян Н.Д., Переверзев А.П. Надлежащая практика фармаконадзора в США и Европейском Союзе. Безопасность и риск фармакотерапии. 2014;(4):23-8. [Merkulov V.A., Bunyatyan N.D., Pereverzev A.P Good Pharmacovigilance practice in the United States and the European Union. Bezopasnost' i risk farmakoterapii. 2014;(4):23-28. (In Russ.)].
  25. Официальный сайт Европейского медицинского агентства, European Medicines Agency. URL: https://www.ema.europa.eu/en Дата обращения/date of access 17.04.2020.
  26. ВОЗ. Мониторинг безопасности лекарств: система сообщений для населения. [WHO. Drug Safety Monitoring: A Communication System for the Public. (In Russ.)]. URL: https://www. who.int/medicines/areas/quality_safety/safety_ efficacy/patient_reporting_safety_monitoringRU. pdf?ua=1. Дата обращения/date of access 17.04.2020.
  27. Официальный сайт Евразийской экономической комиссии. [The official website of the Eurasian Economic Commission. (In Russ.)]. URL: http:// www.eurasiancommission.org. Дата обращения/ date of access 17.04.2020.
  28. Официальный сайт Федеральной службы по надзору в сфере здравоохранения (Росздравнадзора). [The official website of the Federal Service for Supervision of Healthcare (Roszdravnadzor). (In Russ.)]. URL: https://www. roszdravnadzor.ru. Дата обращения/date of access 17.04.2020.

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