Tag: All about ICSR processing
Within this tag, you will discover a complete repository of information pertaining to ICSR (Individual Case Safety Report) cases, presented systematically from top to bottom at each level.
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🍾 Misuse, Abuse & Addiction: An Adverse Event
In this comprehensive blog guide, we uncover the distinctions between misuse, abuse, and addiction as reported in pharmacovigilance, providing clear differentiations with relevant examples.
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🤯 Occupational and Accidental Exposure: An Adverse Event
In this article, we address more complex special case scenarios, such as occupational and accidental exposures, when reported as adverse events.
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🖇 Case Merging: Key Concepts and Criteria Explained
This blog covers: Introduction In this comprehensive blog, we will delve into the nuances and criteria that determine when cases need merging. In one of our previous article, we explored what is a duplicated case and why merging is necessary. Here, we take a deeper look at the key factors that drive the need for…
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👥 Mastering Duplicate Detection: Your Ultimate Guide
In this detailed blog, we delve into the detection of duplicates in pharmacovigilance case processing, incorporating statistical insights throughout our exploration. Join us on our journey as we share our findings and insights.
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➕ Understanding Duplicates in Pharmacovigilance
This blog covers: Introduction Duplicate reports are a regular challenge in pharmacovigilance case processing, encountered by professionals. This blog aims to gain a understanding of duplicates and their global impact on pharmacovigilance datasets. We’ll discuss methods for: What Are Duplicates? Duplicates refer to where a case file exists in many versions, that contains similar information…
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101: Effective Case Book-in Pharmacovigilance: A Step-by-Step Guide 🎟️
Here in this informative pharmacovigilance blog, where we provide a comprehensive overview of the book-in process in Individual Case Safety Report (ICSR) management. In this article, we present a step-by-step guide that simplifies the book-in process, ensuring a better understanding for all.
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📛 Medication Error: An Adverse Event
Discover crucial information on medication error and drug safety in Drugvigil’s blog. Stay informed on pharmacovigilance updates.
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🏁 Case Processing: Initials and Follow-ups Explained
This blog includes: Introduction In adverse event reporting, each case often includes initial reports and multiple follow-ups. This can lead often confusion, when trying to locate the report you are processing. This guide aims to clarify these terms and help you navigate through the complexities of reporting. Definitions Initials Initial reports are the first submissions…
