Abstract Background Due to the limited safety data available at the time that a new medication is first marketed, it is essential to continue the collection and monitoring of safety data about adverse drug reactions (ADRs) during the medication’s life cycle. This activity, known as pharmacovigilance (PV), is performed worldwide by the pharmaceutical industry as well as by regulatory agencies. In 2012, the Israeli Ministry of Health (MOH) established a Pharmacovigilance and Drug Information Department. The Department is tasked with identifying, monitoring, and initiating activities aimed at minimizing risks associated with medication utilization. To enable this, the MOH has devised procedures for PV and promoted extensive legislation in this...
Abstract The Pharmacovigilance department is liable for monitoring the safety of medicines during c...
Pharmacovigilance or drug safety is defined as science and actions related to diagnosis, evaluation,...
Background: Due to the fact that the information about the adverse drug reactions (ADR) registered d...
The overall objectives of Pharmacovigilance include early identification of potential safety hazards...
Department of Pharmacologyand Clinical Pharmacy, SUMPh “Nicolae Testemitanu”, Chisinau, The Republic...
A series of public health disasters (Thalidomide in the 1960s to Rofecoxib (Vioxx) at the beginning ...
An organized Adverse Drug Reaction monitoring program is one mechanism to more actively detect ADRs,...
The role of patients as key contributors in pharmacovigilance was acknowledged in the new EU pharmac...
The mission of the Medicines Authority (MA) in Malta is to contribute to protection of public health...
Published in : Latin American Journal of Pharmacy, 34 (5): 901-6 (2015)SUMMARY. Pharmacovigilance is...
Pharmacovigilance is an activity that provides protection to patients and public health. Problems re...
Introduction. Ensuring the safety of medicines is the basis for the existence and functioning of any...
Pharmacovigilance (PV) plays a key role in the healthcare system through assessment, monitoring and ...
AbstractAdverse Drug Reactions (ADRs) are scantly reported with poor contribution by healthcare prof...
In the 1960s, following the Thalidomide Disaster, the World Health Organization (WHO) initiated the ...
Abstract The Pharmacovigilance department is liable for monitoring the safety of medicines during c...
Pharmacovigilance or drug safety is defined as science and actions related to diagnosis, evaluation,...
Background: Due to the fact that the information about the adverse drug reactions (ADR) registered d...
The overall objectives of Pharmacovigilance include early identification of potential safety hazards...
Department of Pharmacologyand Clinical Pharmacy, SUMPh “Nicolae Testemitanu”, Chisinau, The Republic...
A series of public health disasters (Thalidomide in the 1960s to Rofecoxib (Vioxx) at the beginning ...
An organized Adverse Drug Reaction monitoring program is one mechanism to more actively detect ADRs,...
The role of patients as key contributors in pharmacovigilance was acknowledged in the new EU pharmac...
The mission of the Medicines Authority (MA) in Malta is to contribute to protection of public health...
Published in : Latin American Journal of Pharmacy, 34 (5): 901-6 (2015)SUMMARY. Pharmacovigilance is...
Pharmacovigilance is an activity that provides protection to patients and public health. Problems re...
Introduction. Ensuring the safety of medicines is the basis for the existence and functioning of any...
Pharmacovigilance (PV) plays a key role in the healthcare system through assessment, monitoring and ...
AbstractAdverse Drug Reactions (ADRs) are scantly reported with poor contribution by healthcare prof...
In the 1960s, following the Thalidomide Disaster, the World Health Organization (WHO) initiated the ...
Abstract The Pharmacovigilance department is liable for monitoring the safety of medicines during c...
Pharmacovigilance or drug safety is defined as science and actions related to diagnosis, evaluation,...
Background: Due to the fact that the information about the adverse drug reactions (ADR) registered d...