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Monitoring of Adverse Drug reactions

Monitoring of Adverse Drug reactions of antibiotics in a tertiary care hospital - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/10/058715
Enrollment
345
Registered
2023-10-16
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: 4- Measurement and Monitoring

Interventions

Intervention1: Nil: Nil

Sponsors

Bhagyashree S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients encountered with Adverse Drug Reaction Due to Antibiotics

Exclusion criteria

Exclusion criteria: Pregnant and lactating women. Pediatric patients

Design outcomes

Primary

MeasureTime frame
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. Timepoint: 0 07 14—

Secondary

MeasureTime frame
NilTimepoint: Nil—

Countries

India

Contacts

Public ContactGrinton Josvi Veigas

Karavali College Of Pharmacy

grin2veigas@gmail.com9901751579

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026