Sri Venkateswara Institute of Medical Sciences (SVIMS)
A University established by an Act of Andhra Pradesh State Legislature in 1995 recognized under section 12(B) of UGC


 

 

Pharmacovigilance &

Medical Device Adverse Event Monitoring Centre

 

  1. Pharmacovigilance Committee

  2. Pharmacovigilance Programme of India (PvPI)
  3. Materiovigilance Programme of India (MvPI)

 

Pharmacovigilance Department Insights

Sri Venkateswara Institute of Medical Sciences, Tirupati

Adverse Drug Reaction Monitoring Centre (AMC)

Sri Venkateswara Institute of Medical Sciences, Tirupati, recognized as an Adverse Drug Reaction Monitoring Centre (AMC) and approved by the Indian Pharmacopoeia Commission – National Coordinating Centre (PvPI), Ghaziabad on 08/07/2015, plays a crucial role in safeguarding patient health by systematically monitoring, assessing, and responding to adverse drug reactions (ADRs). With a multidisciplinary team and a strong governance structure, our aim is to enhance the safety and efficacy of medicinal use across the institution.

Objectives of the Pharmacovigilance Committee:

  • Monitor and document adverse drug reactions (ADRs) in inpatient and outpatient settings.

  • Promote awareness and education on drug safety among healthcare professionals.

  • Encourage timely and accurate reporting of ADRs by clinicians, nursing staff, and pharmacists.

  • Analyze data to identify trends, evaluate risk factors, and recommend interventions.

  • Collaborate with the Pharmacovigilance Programme of India (PvPI) and other regulatory bodies.

  • Conduct regular training, workshops, and continuing medical education (CME) programs on pharmacovigilance.

Key Activities:

·           Collection, analysis, and causality assessment of ADR reports from all clinical departments.

·           Conducting monthly Pharmacovigilance Committee meetings to review and discuss the ADRs collected throughout the month.

·           Monthly meetings are held to perform causality assessment of the ADRs by committee experts.

·           Organizing awareness programs and pharmacovigilance workshops for medical and nursing staff.

·           Publishing safety bulletins and updates regarding drug reactions and recalls.

·           Promoting student and intern participation in pharmacovigilance practices.

·           Ensuring confidentiality, integrity, and proper documentation of pharmacovigilance data.

Leadership & Team (PVC Members):

S. No

Name of the Faculty

Designation

PVC Role

01

Dr. Usha Kalawat

Principal

Chairman

02

Dr. R. Ram

Professor & HOD of Nephrology

Co-Chairman

03

Dr. K. Umamaheswara Rao

Professor & HOD of Pharmacology

Co-ordinator

04

Dr. C. Pallavi

Associate Professor of Pharmacology

Deputy Co-ordinator

05

Dr. K. ChandraSekhar

Assistant Professor of Medicine

Member

06

Dr. Y. Mutheeswaraiah

Professor & HOD of General Surgery

Member

07

Dr. K. Vijaya Chandra Reddy

Professor of Pharmacology

Member

08

Dr. Punith Patak

Professor & HOD of Paediatrics

Member

09

Dr. A. Surekha

Associate Professor & I/C HOD, Dermatology

Member

10

Mrs. Prabhavathi

D.D. Nursing

Member

 Junior Pharmacovigilance Associate: Mrs. M.K. Manisha, M. Pharm, appointed by the Indian Pharmacopoeia Commission – National Coordinating Centre (PvPI), Ghaziabad.

Our Commitment:

At SVIMS, pharmacovigilance is not just a regulatory obligation—it is a critical element of clinical care. Through constant vigilance, education, and collaboration, we aim to minimize drug-related harm and continuously improve the standards of patient safety and public health.

***

Medical Device Adverse Event Monitoring Centre

 

We are pleased to announce that our institute has been officially designated as one of the Medical Device Adverse Event (MDAE) Monitoring Centres, with effect from August 23, 2022.

 

As part of this programme:

  • Dr. Ram, Medical Superintendent, has been appointed as the Chairperson of the Monitoring Committee

  • Ms. G. Pavani, Biomedical Technician, will serve as the Coordinator of the MDAE Monitoring Programme

This initiative is a significant step towards enhancing patient safety by systematically reporting and monitoring adverse events related to medical devices. We look forward to active participation and cooperation from all departments to ensure the success of this vital programme.

 

 

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