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Pharmacovigilance

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John Dawod
John Dawod
/
October 21, 2025

Pharmacovigilance

4.87884
4413 Enrolled
Free courses, healthcare, professional development

Welcome to our online course on Pharmacovigilance for healthcare providers in Kenya, a comprehensive and free learning platform designed to enhance your professional skills and knowledge. Our Pharmacovigilance course is offered by CRK clinical research organization and independently sponsored by Pfizer.

Pharmacovigilance, monitoring and assessing medicine safety, is crucial in protecting patient health. Healthcare professionals must stay informed about these practices to manage drug safety effectively.

As a healthcare provider in Kenya, it’s crucial to stay updated with the latest developments in pharmacovigilance. This free course offers you the opportunity to do just that, providing an in-depth exploration of drug safety principles, adverse drug reactions (ADRs), and risk management strategies.

The online course on Pharmacovigilance is tailored to the unique needs and challenges of the Kenyan healthcare system. It delves into the role of regulatory authorities in drug safety, providing you with a comprehensive understanding of the local and global pharmacovigilance landscape.

Our course is not just about theory; it’s about practical application. You’ll learn how to identify, assess, understand, and prevent adverse drug reactions, enhancing patient safety and improving treatment outcomes. The knowledge and skills you gain will directly apply to your daily practice, making you a more effective and informed healthcare provider.

Enroll in our online course on Pharmacovigilance for healthcare providers in Kenya and take the next step in your professional journey.

 

 

What Will I Learn?

  • Understanding the Pharmacovigilance System in Kenya
  • Identifying and Reporting ADRs in Specific Medical Areas
  • Strategies for Managing and Preventing ADRs
  • Effective Communication with Patients on ADR Reporting
  • Reporting ADRs in Pediatric Populations
  • Building Pharmacovigilance Systems in Resource-Limited Settings

Course Content

Module 1: Understanding the Pharmacovigilance System in Kenya
This module provides a comprehensive overview of the pharmacovigilance system in Kenya, highlighting its significance in ensuring patient safety and the regulatory framework governing it. It is divided into three key lessons that cover different aspects of pharmacovigilance:Lesson 1: Introduction to Pharmacovigilance and Its Importance in Patient Safety In this introductory lesson, learners gain a fundamental understanding of pharmacovigilance and its vital role in safeguarding patient health and well-being. It explores the concept of adverse drug reactions (ADRs) and emphasizes the need for systematic monitoring and reporting to identify and mitigate potential risks associated with pharmaceutical products.Lesson 2: Pharmacovigilance Regulations and Reporting Requirements in Kenya This lesson delves into the specific regulatory landscape of pharmacovigilance in Kenya. It outlines the legal framework and reporting obligations that pharmaceutical companies, healthcare professionals, and other stakeholders must adhere to. Topics covered include regulatory agencies, timelines for reporting, and non-compliance consequences.Lesson 3: Methods of Adverse Drug Reaction (ADR) Reporting The final lesson explores the various methods and channels for reporting adverse drug reactions in Kenya. It provides insights into the different reporting mechanisms, including spontaneous reporting by healthcare professionals and patients, as well as the role of pharmacovigilance centers and online reporting portals. Learners will understand the importance of accurate and timely reporting in building a robust pharmacovigilance system.In summary, Module 1 offers a holistic understanding of the pharmacovigilance system in Kenya, starting with its fundamental principles and expanding into the regulatory framework and practical reporting mechanisms. This knowledge equips learners with the necessary tools to enhance drug safety and patient care in the country.

  • Module 1 pre-test
  • Module 1 Overview
    00:00
  • Lesson 1: Introduction to Pharmacovigilance and Its Importance in Patient Safety
    08:40
  • Lesson 2: Pharmacovigilance Regulations and Reporting Requirements in Kenya
    06:36
  • Module 1 lesson 2 (Roleplay)
    03:04
  • Lesson 3: The process of reporting pharmacovigilance in Kenya
    15:47
  • Module 1 lesson 3 (Roleplay) Reporting Methods
    03:28
  • Module 1 Assessment Test

Module 2: Identifying and Reporting ADRs in Specific Medical Areas
Welcome to Module 2 of our Medical Education Program on Adverse Drug Reaction (ADR) Reporting. This module will explore ADR reporting in specific medical areas and understand the importance of early detection and intervention to ensure patient safety. Let's get started with Lesson 1: ADR Reporting in Oncology. Lesson 1: ADR Reporting in Oncology: Case Studies and Best Practices This lesson will focus on ADR reporting in oncology, where patients undergo cancer treatment with various medications. We will examine real-life case studies highlighting the significance of ADR reporting in early detection and intervention. Additionally, we will discuss best practices for accurate and efficient ADR reporting in oncology. Lesson 2: ADR Reporting for Vaccines: Ensuring Vaccine Safety in Kenya Lesson 2 will revolve around ADR reporting for vaccines, an essential aspect of ensuring vaccine safety in Kenya. Vaccines play a critical role in preventing infectious diseases, and ADR reporting is vital to monitor and address any potential adverse effects associated with vaccination. Lesson 3: ADR Reporting for Anti-hypertensive Medications: Managing Cardiovascular Risks In Lesson 3, we will focus on ADR reporting for anti-hypertensive medications. Hypertension, or high blood pressure, is a prevalent condition, and proper ADR reporting is crucial in managing cardiovascular risks and optimizing treatment outcomes. Lesson 4: ADR Reporting for Neglected Non-communicable Diseases Medications Lesson 4 will explore ADR reporting for neglected non-communicable diseases (NCDs) medications. These medical conditions have historically received limited attention, making ADR reporting even more critical in improving patient care and safety. Case Studies: Identifying ADRs in Oncology and Reporting Correctly In these case studies, we will explore scenarios where healthcare providers must identify ADRs in oncology patients accurately and report them correctly. Through interactive activities, we will enhance our understanding of the challenges and importance of ADR reporting in oncology. Case Study: Identifying and Reporting ADRs in Vaccines and Anti-hypertensive Medications In this case study, we will face scenarios related to vaccine administration and anti-hypertensive medication use. By actively participating in this case study, we will practice recognizing ADRs and reporting them appropriately to ensure patient safety. Lesson 5: Identifying and reporting adverse events in endemic communicable diseases in Kenya (TB, HIV/AIDS, and malaria): case studies and hands-on training on properly completing adverse event reports for neglected endemic communicable disease medications. Learning Objectives: 1. Understand the significance of adverse drug reaction (ADR) reporting in specific medical areas, recognizing its role in improving patient safety and treatment outcomes. 2. Identify common adverse drug reactions associated with medications used in specific medical areas, such as cardiology, neurology, and infectious diseases. 3. Recognize the challenges and complexities of ADR reporting in specialized medical fields, including polypharmacy, overlapping symptoms, and patient variability. 4. Implement best practices for ADR reporting in specific medical areas, including timely reporting, utilizing common terminology and grading scales, and collaborating with multidisciplinary teams. 5. Utilize technology and data collection methods to streamline ADR reporting processes in specialized medical fields and contribute to pharmacovigilance efforts. 6. Comprehend the ethical considerations in ADR reporting, including patient confidentiality, informed consent, and reporting of uncertain causality or rare events. 7. Foster a culture of reporting in specific medical areas, overcoming barriers to reporting and encouraging healthcare professionals' engagement and patient involvement. Interactive Activities: 1. Case Studies and Discussion: Participants will be presented with real-life case studies of adverse drug reactions in specific medical areas, such as cardiology, neurology, and infectious diseases. They will discuss the implications of these ADRs on patient health and treatment decisions and brainstorm possible reporting strategies and interventions. 2. Interactive Quizzes: Throughout the module, interactive quizzes will be conducted to reinforce participants' understanding of ADR reporting in specific medical areas. These quizzes will cover topics such as best practices, terminology, and technology utilization. 3. Role-Playing animation videos: to simulate ADR reporting scenarios in specialized medical fields. They will practice communication with patients about potential ADRs and report to pharmacovigilance centers. 4. Technology Demonstration: A demonstration of technology tools and software used for ADR reporting in specific medical areas will be provided. Participants will learn how to use these tools to streamline reporting processes and improve data collection. By incorporating these interactive activities into the module, participants can apply their knowledge, engage in discussions, and develop practical skills related to ADR reporting in specialized medical fields. These activities will enhance participants' understanding of the importance of ADR reporting, equip them with effective reporting strategies, and foster a culture of vigilant pharmacovigilance in specific medical areas. Throughout this module, we encourage active engagement and discussion. Let's work together to improve our knowledge and skills in ADR reporting for specific medical areas, ultimately enhancing patient care and promoting safer healthcare practices. Let's embark on this learning journey together!

Module 3: Strategies for Managing and Preventing ADRs
• Lesson 1: Understanding Adverse Drug Reactions and Their Management • Lesson 2: Preventing ADRs: Strategies for Safer Medication Use • Lesson 3: Implementing Risk Minimization Measures • Assignment: Develop a Risk Minimization Plan for a Specific Medication

Module 4: Effective Communication with Patients on ADR Reporting
• Lesson 1: Importance of Patient Communication in ADR Reporting • Lesson 2: Communicating ADRs to Patients and Their Families: Best Practices • Quiz: Assessing Communication Skills in ADR Reporting

Module 5: Reporting ADRs in Pediatric Populations

Module 6: Building Pharmacovigilance Systems in Resource-Limited Settings

About the instructors

John Dawod

John Dawod

John Heshmat is a pharmacist and public health professional with over a decade of diverse experience in clinical research, health education, and humanitarian service across Africa. He holds a Master’s in International Public Health from Liverpool John Moores University and a Bachelor of Pharmacy from October 6 University.

As the Clinical Operations Manager at CRK Clinical Research Key (CRO), John leads high-impact clinical research and capacity-building programs targeting underserved populations in Kenya. He also serves as the Country Coordinator for Mécénat Chirurgie Cardiaque, a global organization that sponsors life-saving heart surgeries for children with congenital heart defects.

At CRKCourses.com, John combines scientific rigor with practical field insight to deliver CME/CPD-accredited e-learning programs for healthcare professionals. His teaching emphasizes evidence-based practice, health equity, and the real-world application of research in resource-limited settings.

With a passion for public service and training the next generation of African health leaders, John is committed to improving patient outcomes through education, innovation, and collaborative learning.

 4.86 (1336 ratings)

4 Courses

8719 students

crk.cro

crk.cro

CRK is Kenyan’s largest and most comprehensive provider of post-graduate training courses in clinical research, public health, pharmaceutical sciences, and various other domains. At CRK-CRO, we believe a properly trained and competent health workforce is essential to any successful healthcare system.

 4.81 (1763 ratings)

10 Courses

1509 students

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884 Reviews
CS

great information

LW

Very detailed course and a good refresher

MI

Very nice

KA

good

PW

Good well-presented course

MV

learnt new stuff

CA

The content was well presented . The role playing videos were great for understanding the content better.

MM

It was great

BO

Great experience

PK

I had an incredible experience that expanded my knowledge and provided me with valuable insights into Pharmacovigilance.

Free
Free access this course
  • 4413 Total Enrolled
  • Certificate of completion
Durations:
Lectures: 36
Students: Max 0
Level: Intermediate
Language: English
Certificate: Yes

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