None listed
Conditions
Interventions
Intervention1: NIL: NIL
Control Intervention1: NIL: NIL
Sponsors
Dr Aditya V
Eligibility
Inclusion criteria
Inclusion criteria: The community and hospital pharmacist in North Bengaluru India who give their informed consent will be included in the study.
Exclusion criteria
Exclusion criteria: Participants who do not provide their consent will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The outcome will be measured using a suitable self-administered questionnaire designed by referring similar kinds of literatures with input from the experts using both open and closed ended questions and some modifications were made to the questionnaire which is used to compare the knowledge, attitude and practice of Pharmacovigilance and Adverse Drug Reaction reporting among hospital pharmacist and community pharmacists in North Bengaluru India.Timepoint: At baseline 4 weeks 8 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| The outcome will be measured using a suitable self-administered questionnaire designed by referring similar kinds of literatures with input from the experts using both open & closed ended questions & some modifications were made to the questionnaire which is used to evaluate knowledge, attitude, practice & future perspective on Pharmacovigilance & Adverse reaction reporting among hospital pharmacist & community pharmacists in North Bengaluru India.Timepoint: At baseline 2 weeks 6 weeks | — |
Countries
India
Contacts
Public ContactSrilakshmi R Bhat
Gautham College of Pharamcy
Outcome results
None listed