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Monitoring of Adverse Drug reactions

Not Applicable
Conditions
Health Condition 1: 4- Measurement and Monitoring
Registration Number
CTRI/2023/10/058715
Lead Sponsor
Bhagyashree S
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients encountered with Adverse Drug Reaction Due to Antibiotics

Exclusion Criteria

Pregnant and lactating women.

Pediatric patients

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
This study will help to monitor adverse drug reaction caused by antibiotics,to study the prevalence and pattern of ADRs and to assess the severity, outcomes of ADR’s. <br/ ><br>Timepoint: 0 07 14 <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
ilTimepoint: Nil
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