Adverse Drug Reactions and Drug Safety
Monitoring adverse drug reactions (ADRs) is essential for ensuring drug safety. ADRs, ranging from mild effects to severe toxicity, can result from drug interactions, genetic factors, or dosage errors. Pharmacovigilance systems have evolved to track ADRs post-marketing, enabling early detection of risks. Personalized medicine, through pharmacogenomics, improves drug safety by predicting individual responses to therapies, minimizing ADRs, and optimizing treatment. Regulatory frameworks also play a crucial role in maintaining drug safety.
Related Conference of Adverse Drug Reactions and Drug Safety
December 18-19, 2024
3rd International Conference and Expo on Medical Toxicology and Applied Pharmacology
Zurich, Switzerland
March 10-11, 2025
12th International Conference on Pollution Control & Sustainable Environment
Rome, Italy
Adverse Drug Reactions and Drug Safety Conference Speakers
Recommended Sessions
- Advances in Anticancer Drug Toxicology
- Advances in Clinical Toxicology
- Adverse Drug Reactions and Drug Safety
- Analytical Techniques in Toxicology
- Antidote Development and Therapeutic Interventions
- Cardiotoxicity and Drug-Induced Cardiac Disorders
- Drug Overdose and Poisoning Management
- Environmental and Occupational Toxicology
- Forensic Toxicology and Legal Aspects
- Genotoxicity, Carcinogenicity, and Mutagenesis
- Hepatotoxicity and Drug-Induced Liver Injury
- Molecular Mechanisms of Toxicity
- Neurotoxicology and Neuropharmacology
- Pesticides and Industrial Chemicals Toxicology
- Pharmacokinetics and Drug Metabolism
- Regulatory Toxicology and Public Health Implications
- Renal Toxicity and Nephrotoxicity
- Risk Assessment in Toxicology
- Toxicokinetics and Toxicodynamics
- Toxicology of Nanoparticles and Emerging Contaminants
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