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Risk-benefit analysis is a process used to evaluate the potential risks and benefits associated with a decision or action, helping to determine whether the benefits outweigh the risks. It is a critical tool in decision-making across various fields, ensuring that potential negative outcomes are carefully weighed against expected positive outcomes.
Adverse effects are unintended, harmful outcomes that occur as a result of medical treatment or intervention, which can range from mild to severe. Understanding and managing these effects is crucial for patient safety, drug development, and regulatory compliance in healthcare.
Dosage optimization is a process in pharmacology and medicine that aims to determine the most effective dose of a drug that maximizes therapeutic benefits while minimizing adverse effects. It involves a balance of pharmacokinetics, pharmacodynamics, patient-specific factors, and clinical outcomes to ensure safe and effective treatment.
Patient safety is a fundamental principle of healthcare that aims to prevent harm to patients during the provision of health services. It involves the establishment of systems and processes to minimize errors and adverse events, ensuring high-quality and reliable care.
Pharmacology is the branch of medicine that focuses on the study of drugs and their effects on living organisms, encompassing the development, chemical properties, and therapeutic applications of pharmaceutical agents. It plays a crucial role in understanding how drugs interact with biological systems to treat, prevent, or diagnose diseases, ensuring their safety and efficacy.
The therapeutic index is a ratio that compares the toxic dose of a drug to its effective dose, providing a measure of drug safety. A larger therapeutic index indicates a greater margin between effective and toxic doses, suggesting a safer drug profile.
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