Pharmacovigilance
Pharmacovigilance
Adverse Drug Reactions (ADRs)
Monitoring and evaluating any unwanted or harmful effects experienced by patients after taking a medication.
Data Collection
Gathering information from various sources, including patients, healthcare providers, and medical literature, to identify and analyze adverse effects.
Regulatory Reporting
Submitting adverse event data to local and international drug regulatory authorities to ensure transparency and compliance with legal requirements.
Risk Assessment
Evaluating the risks associated with pharmaceutical products to determine their safety profile.
Risk Management
Implementing strategies to minimize the risk of adverse effects, such as revising dosage recommendations, issuing warnings, or withdrawing unsafe drugs from the market.
Public Health Protection
Ensuring that the benefits of a drug outweigh its risks and communicating safety information to healthcare professionals and the public.
