Study of adverse drug reactions to antiretroviral therapy in a tertiary care hospital, Tirupati
Autor: | Ramesh Babu Atmakuru, Rajalakshmi Rukmangathen, Vasundara Devi Brahmanapalli, Sai Deepak Gali, Deepishka Pemmasani, Durga Prasad Thammisetty |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
Efavirenz Nevirapine lcsh:Medicine 030226 pharmacology & pharmacy 03 medical and health sciences chemistry.chemical_compound Zidovudine 0302 clinical medicine Internal medicine Pharmacovigilance Medicine 030212 general & internal medicine Adverse effect adverse drug reactions lcsh:R5-920 business.industry Incidence (epidemiology) lcsh:R Lamivudine General Medicine highly active antiretroviral therapy Regimen chemistry pharmacovigilance Original Article business lcsh:Medicine (General) medicine.drug |
Zdroj: | Perspectives in Clinical Research, Vol 11, Iss 4, Pp 158-163 (2020) Perspectives in Clinical Research |
ISSN: | 2229-3485 |
Popis: | Purpose: Human immunodeficiency virus-infected patients do not adhere to their antiretroviral therapy (ART) due to adverse effects of drugs. The continuous monitoring of adverse drug reactions (ADRs) may ensure the safe use of drugs in patients. Hence, a retrospective analysis was carried out to assess the ADRs pattern, causality, and severity associated with various antiretroviral drug regimens in patients receiving ART. Materials and Methods: A retrospective, analytical study was carried out at ART nodal center in Sri Venkateswara Ramnarain Ruia Government General Hospital, Tirupati. Data were collected by spontaneous reporting of health-care professionals from ART centers using Suspected ADR Reporting Forms of Indian Pharmacopoeia Commission to record the ADRs occurred in the patients who underwent treatment from December 2015 to November 2016. A total of 299 ADR reports were collected during the study period. The causality and severity of the reported ADRs were assessed using suitable scales. Results: From a total of 299 ADR reports, females (63.81%) experienced higher ADRs than males (36.12%). The highest number of ADRs was reported to zidovudine/lamivudine/nevirapine (ZLN) regimen (76.92%) than tenofovir/lamivudine/efavirenz (TLE) regimen (23.07%). Cutaneous reactions were higher (34.34%) among patients receiving ZLN therapy, and drowsiness (53.62%) was the most common ADR in patients receiving TLE regimen. According to the World Health Organization causality assessment scale, most of the ADRs were possible (75.92%). On the assessment of Modified Hartwig and Siegel Severity Scale, 55.09% of ADRs were moderate. Conclusion: The study showed an increased incidence of ADRs to ART which calls for efficient pharmacovigilance systems to improve patient care and drug safety. |
Databáze: | OpenAIRE |
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