The Indian Pharmacopoeia Commission (IPC) celebrates the National Farmacovigilance Sunday starting September 17-23 to increase awareness about the safety profile of medical products, including drugs, medical devices and vaccines, to maintain public health.
On this occasion, AIIMS Nagpur shares important information about Farmacovigilance.
Farmacovigilance (PV) ‘Farmacon’ (Greece), which means’ drug ‘vigilare’ (Latin), which means’ to stay awake or alert ‘,’ to continue watching ‘why PV is needed India is currently the largest drug manufacturer 4th above 60,000.
The branded formulation is available in the drug reaction to the market (ADRS) of 0.7% ADR hospitalization responsible for 1.8% of deaths among total hospital admission many medical devices bring reactions, problems to patients who report the problem in such situations It is to enhance the medical device reporting experience requires a medical device commonly used: stent heart, glucometer, internal prostetic replacement, automatic external defibrillator (AED), orthopedic implants, disposable syringes and syringes such as drugs, medical devices also contain possibilities Threats and risks in the application and / or implementation of instruments, equipment, implants, reagents or in vitro software intended for diagnosis or treatment of diseases can be reported pH of the Indian Armacovogilace PH (PVPI) program and the Indian Materials (MVPI) program (MVPI) of the Central Government and IPC initiated the program National PV in 2010.
MVPIWAS was launched In the 2015 PVPI what detected ADR was new, delayed and rare ADR from reported cases.
Monitor Benefits – Risk Profiles of drugs that produce independent recommendations, evidence-based about the safety of drugs Supporting standard drug control organizations in formulating regulated regulatory decisions for drugs that can report ADR health professionals: Doctors, Dentists, Dentists, Dentists, Dentists Professional Nurses Nurse Staff Health Care: Counselors, patients, servants What will report all side effects associated with ADR new drugs and established because of ADR’s error related to the withdrawal of drugs.
The lack of efficacy / alleged pharmaceutical defects the impact of unexpected drugs and drug food supplement interactions how and who reports to heal professionals, patients or other people can report ADR to the monitoring center of the nearest drug reaction (AMC) PVPI has more than 395 AIims Nagpur Also your AMC must fill out the form of ‘allegations of detrimental drug reactions’ a person’s form can directly e-mail ADR to PVPI @ ipcindia.net / pvpi.ipcindia @ gmail.com Speak it is very important to monitor side effects related to drugs and devices Medical through strong, sustainable and scale supervision.
Citizens can help us in raising awareness about drugs and medical devices from Ganesh Dakhale | Professor and PVPI Coordinator, Department of Pharmacology, AIIMS Nagpur