"Pharmacovigilance is the science and activities relating to the
detection, assessment, understanding and prevention of adverse effects
or any other medicine-related problem" -WHO
This Program for International Drug Monitoring was established by WHO as a result of the thalidomide disaster detected in 1961. Pharmaceutical manufacturing companies are required by law in all countries to perform clinical trials, testing new drugs on people before they are made generally available in the market. At the end of 2010, 134 countries were part of the WHO Pharmacovigilance (PV) Programme.
The Purpose of Pharmacovigilance
In today's advanced age of medicines, science and technology, there has been an increasing public awareness of safety issues related to medical products. This has led to an increased importance of pharmacovigilance.
This Program for International Drug Monitoring was established by WHO as a result of the thalidomide disaster detected in 1961. Pharmaceutical manufacturing companies are required by law in all countries to perform clinical trials, testing new drugs on people before they are made generally available in the market. At the end of 2010, 134 countries were part of the WHO Pharmacovigilance (PV) Programme.
The Purpose of Pharmacovigilance
- The main purpose of pharmacovigilance is to improve the patient's safety and enhance his care in terms of the use of medicines, including paramedical interventions.
- Pharmacovigilance also supports public health programs by providing reliable information for the efficient assessment of the risk-benefit profile of medicines.
- Contribute to the assessment of benefits, uses, side effects, harm, effectiveness and risk of medicines.
- Encouraging the safe, rational and more effective (including cost-effective) use of various medicines.
- Promote education, understanding and clinical training in pharmacovigilance and its effective availability to the public.Recently, pharmacovigilance has widened its horizon to include:
- Traditional and complementary medicines
- Herbals
- Biologicals
- Blood products
- Medical devices
- Vaccines
- Drug monitoring
- Pharmaceutical preparations - adverse effects
- Adverse drug reaction reporting
- Product surveillance
- Postmarketing Legislation
- Medication errors
- Substandard medicines
- Lack of efficacy reports
- Use of medicines that are not approved for
- Case reports of acute and chronic poisoning
- Study of drug-related deaths
- Abuse and misuse of medicines
- Adverse affects of medicines with chemicals, other medicines, and food.
In today's advanced age of medicines, science and technology, there has been an increasing public awareness of safety issues related to medical products. This has led to an increased importance of pharmacovigilance.
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