Bioequivalence and Bioavailability Forum • Adverse Event Reporting

Adverse Event Reporting [Regulatives / Guidelines]

posted by such – 2008-09-09 16:37 (6490 d 15:27 ago) – Posting: # 2341
Views: 5,173

Hello friends,

Can any one tell me if

A subject has experienced an adverse event of mild severirty for first two days and then it progressed into moderate severity AE then while reporting are they considered as two different events or single event and how should they be captured in CRF?

Thanks,

Such

Complete thread:

Adverse Event Reportingsuch 2008-09-09 14:37 [Regulatives / Guidelines]
- Adverse Event Reporting Ohlbe 2008-09-09 17:14
  - Adverse Event Reporting such 2008-09-10 08:46
    - Adverse Event Reporting Ohlbe 2008-09-10 10:30
      - Adverse Event Reporting such 2008-09-10 11:42
        
        Adverse Event Reporting Ohlbe 2008-09-10 11:56