Chapter 2
Adverse Drug Effects and Chemical Toxicity
Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a…
Medications are typically administered to achieve therapeutic effects. Some drugs can modify an individual's mood and perception, frequently…
Humans continually engage with an environment rich in potentially harmful chemicals. These are introduced to our bodies through inhalation,…
When toxic substances penetrate the human body, they disseminate to various tissues, undergoing metabolic changes. This process yields reactive…
The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity,…
Mutagenicity and carcinogenicity refer to the ability of drugs to cause genetic defects and induce cancer, respectively. The International Agency for…
Human Liver Microphysiological System for Assessing Drug-Induced Liver Toxicity In Vitro
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DILI is a major cause of attrition in drug development with over 1000 FDA-approved drugs known to potentially cause DILI in humans. Unfortunately,…
Basophil Activation Test for Investigation of IgE-Mediated Mechanisms in Drug Hypersensitivity
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Hypersensitivity reactions against non-steroidal anti-inflammatory drugs (NSAIDs) like propyphenazone (PP) and diclofenac (DF) can manifest as Type…