bioRxiv preprint doi: https://doi.org/10.1101/358069; this version posted June 28, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 1 Original Manuscript 2 Title: Antiretroviral Adverse Drug Reactions Pharmacovigilance in Harare City, 3 Zimbabwe, 2017 4 Hamufare Mugauri1, Owen Mugurungi2, Tsitsi Juru1, Notion Gombe1, Gerald 5 Shambira1 ,Mufuta Tshimanga1 6 7 1. Department of Community Medicine, University of Zimbabwe 8 2. Ministry of Health and Child Care, Zimbabwe 9 10 Corresponding author: 11 Tsitsi Juru
[email protected] 12 Office 3-66 Kaguvi Building, Cnr 4th/Central Avenue 13 University of Zimbabwe, Harare, Zimbabwe 14 Phone: +263 4 792157, Mobile: +263 772 647 465 1 bioRxiv preprint doi: https://doi.org/10.1101/358069; this version posted June 28, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 15 Abstract 16 Introduction: Key to pharmacovigilance is spontaneously reporting all Adverse Drug 17 Reactions (ADR) during post-market surveillance. This facilitates identification and 18 evaluation of previously unreported ADR’s, acknowledging the trade-off between 19 benefits and potential harm of medications. Only 41% ADR’s documented in Harare 20 city clinical records for January to December 2016 were reported to Medicines 21 Control Authority of Zimbabwe (MCAZ).