Ayurvedic Pharmacovigilance study
Not Applicable
Completed
- Conditions
- Health Condition 1: null- A prospective, observational study was conducted over a period of 1 year
- Registration Number
- CTRI/2010/091/001164
- Lead Sponsor
- o sponsorship
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 250
Inclusion Criteria
All OPD and IPD patients of KLE Ayurveda hospital, presenting with the ADR (as per WHO definition)
Exclusion Criteria
Patients with intentional and accidental poisoning will be excluded
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method vomiting, nausea, diarrhea, rashes, fewer etc.Timepoint: immediate, 30mins, 1hour, 6hour, upto 45days
- Secondary Outcome Measures
Name Time Method Chronic drug eventsTimepoint: up to 6-months