Adverse Drug Reactions: Types and Classifications Explained

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🕒: 4 min

This blog features:

  1. Definitions
  2. Various types of Adverse drug reactions
  3. Key takeaways included

Introduction

In this comprehensive series of blogs we discussed plenty of times about adverse events and adverse reactions. So to continue exploring that we discuss here with the different types of ADR and with comprehensive definitions added.

Since you might of think ADR is just a term but it varies by its significance of its effect on our human body. Likewise what we see earlier about the grades of adverse events as by CTCAE.

📢 Recommendation: To dig further more to clarify this content by variations between adverse event and adverse drug reactions.

Types of ADR

Below are the list that could be classified of ADRs based on its effects:

  1. Type A effects
  2. Type B effects
  3. Type C effects
  4. Type D effects
  5. Type E effects
  6. Type F effects

Type A effects

  • It is dose dependent and predictable are those due to exaggerated pharmacological effects.
  • Fairly common and dose related
  • Can be avoided by adjusting or using doses

Type B effects

  • Dose independent and unpredictable
  • Bizarre effects or idiosyncratic
  • Occurs less amount of patient
  • Little or no relation with doses
  • Either immunological or non-immunological
Immunological reactions

Immunological reactions may range from rashes, anaphylaxis, vasculitis, inflammatory organ injury, to highly specific autoimmune syndromes.

Non-immunological

This effects may occurs in minority of predisposed, intolerant, patients, because of an inborn error of metabolism or acquired deficiency in a certain enzyme.

“Every adverse drug reaction is a reminder that healing and harm often share the same path — vigilance turns uncertainty into safety.”

Type C effects

  • It is a chronic effects
  • It may be both serious and common
  • It may be coincidental and often concern long term effects

Type D effects

  • Delayed effects (dose independent)
  • Carcinogenicity (e.g., immunosuppressants)
  • Teratogenicity (e.g., fetal hydantoin syndrome)

Type E effects

End-of-treatment effects

Type F effects

Failure of therapy

📢 Recommendation: Click the link here, to explore in deeper about nuances of adverse event and how to proceed in pharmacovigilance and processing.

Key takeaways

ADRs are not just limit one that we say, differ in deep analysis

Every effect has its uniqueness in terms of reactions

Even therapy failues can be considered under ADRs

“Don’t just comply. Lead in pharmacovigilance.”

At Drugvigil, we believe compliance is only the foundation — true excellence begins when you go beyond it.

With robust case management, literature monitoring, signal detection, and MedDRA expertise, we help you ensure not just compliance — but confidence, clarity, and leadership in patient safety.

Conclusion

From the above write up, it is a little overview of detailing the adverse reaction is not simply as one. It has different variations that characterised by different situations and occurennces and results of ths conditions.

Share this pice of content with anyone who are interested with exploring adverse reactions that are need to explore in detail.

Feel free to comment your suggestions and share with your colleagues and friends.

Disclaimer: We write this blog based on our experience and extensive knowledge, supported by references. Please note that we are not responsible for the content on the referenced websites. If you come across any misinformation or misguidance or spelling mistakes, kindly inform us promptly.



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Meet Bala, the founder of Drugvigil, a service provider specializing in pharmacovigilance. He’s not only an expert in this field, but also a passionate entrepreneur who enjoys creating new opportunities and helping others grow. Despite starting from scratch, he’s determined to develop his company from the ground up. If you’re interested in his work, be sure to show your support and share his message with others.




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