Unit 1
Pharmacovigilance and Adverse Drug Reactions
NotesPDF · 429 KB
Complete unit or chapter notes PDFs
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Unit 2
Drug Classification, Coding and Pharmacovigilance Resources
NotesPDF · 352 KB
Unit 3
Vaccine Safety Surveillance
NotesPDF · 369 KB
Unit 4
Safety Data, ICH Guidelines and ADR Pharmacogenomics
NotesPDF · 549 KB
Unit 5
Drug Safety in Special Populations
NotesPDF · 627 KB
Video lessons
Choose a unit and watch FirstHope lessons on YouTube.
Unit 1Introduction to pharmacovigilance and adverse reactions3 videos
Introduction to pharmacovigilance | B Pharm 8th sem
Introduction to adverse drug reactions | Pharmacovigilance | B Pharm 8th sem
Basic terminologies used in pharmacovigilance | B Pharm 8th sem
Unit 2Classification, coding and pharmacovigilance programmes3 videos
Drug and Disease Classification | Pharmacovigilance | B Pharm 8th Sem
Drug Dictionaries, Coding and Information Resources | Pharmacovigilance | B Pharm 8th Sem
Establishing a Pharmacovigilance Program | Pharmacovigilance | B.Pharm 8th Sem
Unit 3Vaccine safety, surveillance methods and communication3 videos
Vaccine safety surveillance | Pharmacovigilance | B Pharm 8th sem
Pharmacovigilance Methods | B Pharm 8th Sem
Communication in Pharmacovigilance | B Pharm 8th Sem
Unit 4Safety data and ICH guidance2 videos
Safety data generation | Pharmacovigilance | B Pharm 8th sem
ICH guidelines for pharmacovigilance | B Pharm 8th sem
Unit 5Pharmacogenomics and special populations2 videos
Pharmacogenomics of adverse drug reactions | Pharmacovigilance | B Pharm 8th sem
Drug safety evaluation in special populations | Pharmacovigilance | B Pharm 8th sem
PYQ & Important Questions
Prepare for Pharmacovigilance.
Previous Year Questions
PYQs for this subject will be added later.
Important Questions
Original subject-specific practice questions for revision.
- Distinguish an adverse event from an adverse drug reaction and a medicine-safety signal.
- Explain the purposes of standardised drug and disease coding.
- Describe how vaccine-safety surveillance addresses suspected adverse events.
- Discuss the importance of complete safety reports and pharmacovigilance quality systems.
- Explain how genetic variation may influence adverse drug reactions.
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