A two-year retrospective observational study of adverse drug reactions related to intravenous drug formulations

Authors

  • Ramani Gade Kamineni Institute of medical sciences, Narketpally, Nalgonda,Telangana,India Author
  • Shivaraj B Patil Narketpally, Nalgonda,Telangana,India Author
  • Shivaraj B Patil Kamineni Institute of medical sciences, Narketpally, Nalgonda,Telangana,India Author
  • Venkata Rao Y Kamineni Institute of medical sciences, Narketpally, Nalgonda,Telangana,India Author
  • Raghuveer B Kamineni Institute of medical sciences, Narketpally, Nalgonda,Telangana,India Author
  • Yamini V Kamineni Institute of medical sciences, Narketpally, Nalgonda,Telangana,India Author
  • Sindhu P Kamineni Institute of medical sciences, Narketpally, Nalgonda,Telangana,India Author

Keywords:

Adverse drug reactions, intravenous products, spontaneous report, NCC-PvPI, WHOUMC causality scale

Abstract

Introduction: Adverse drug reactions are the major obstacles to patient safety and drug therapy monitoring.

Objectives: The present article provides information on intravenous products induced adverse drug reactions collected by spontaneous reporting method through an established pharmacovigilance wing working under NCC-PVPI in an Adverse Drug reaction monitoring center-Nalgonda, Telangana.

Methods: A total number of 100 intravenous products induced ADRs were collected from different age groups by observational retrospective study for the year January 2018 to December 2019.

Results: The results showed that the most affected age group was 20-29 yrs (28 %). The major contribution of the gender that exposed to ADRs was female- 73 % Most intravenous product induced ADRs were reported from the Department of OBG (46 %). Drug: Ceftriaxone-induced ADRs were (38 %). The most frequently reported ADR was fever and chills (56 %). Out of 100 ADRs, one was certain, 90 were probable/likely, and the remaining 9 were possible as per the WHO-causality scale.

Conclusions: In the present work, most of the ADRs were because of intravenous antibiotics followed by anesthetic agents, antiepileptic drugs, ringer lactate, dextrose normal saline, and H2 blockers.

Author Biographies

  • Ramani Gade, Kamineni Institute of medical sciences, Narketpally, Nalgonda,Telangana,India

    Department of pharmacology

  • Shivaraj B Patil, Narketpally, Nalgonda,Telangana,India

    Kamineni Institute of medical sciences

  • Shivaraj B Patil, Kamineni Institute of medical sciences, Narketpally, Nalgonda,Telangana,India

    Department of pharmacology

  • Venkata Rao Y, Kamineni Institute of medical sciences, Narketpally, Nalgonda,Telangana,India

    Department of pharmacology

  • Raghuveer B, Kamineni Institute of medical sciences, Narketpally, Nalgonda,Telangana,India

    Department of pharmacology

  • Yamini V, Kamineni Institute of medical sciences, Narketpally, Nalgonda,Telangana,India

    Department of pharmacology

  • Sindhu P, Kamineni Institute of medical sciences, Narketpally, Nalgonda,Telangana,India

    Department of pharmacology

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Published

2021-03-01

How to Cite

A two-year retrospective observational study of adverse drug reactions related to intravenous drug formulations. (2021). Journal of Pharmacovigilance and Drug Research, 2(1), 22-26. https://test.jpadr.com/index.php/jpadr/article/view/19

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