A novel scale to assess the causality of adverse events
Not Applicable
- Registration Number
- CTRI/2022/06/043595
- Lead Sponsor
- ACTREC Tata Memorial Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Children and adults having an adverse event/s in the past 7 days
2. Having a valid prescription for an approved allopathic drug/s
3. Having adequate documentation of antecedent medical conditions including
comorbidities
4. Having adequate documentation of other drugs, including complementary and
alternative medicines (CAM), administered in the last one month.
Exclusion Criteria
1. Patients receiving an investigational medicinal product.
2. Patients not willing to give a written informed consent.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method