An adverse drug reaction (ADR) is defined as "a considerably detrimental or unpleasant reaction arising from an intervention related to the use of a therapeutic agent; adverse effects typically anticipate hazards from future administration and warrant prevention, specific treatment, dosage regimen modification, or product withdrawal." An adverse event happens when a patient suffers injury while taking a drug, regardless of whether the drug is suspected of being the cause. ADRs generate a significant proportion of hospital admissions, and hospitalised patients regularly have ADRs that complicate and lengthen their stay. Many of these ADRs can be avoided by exercising greater caution. An ADR usually necessitates the drug's discontinuation or dosage reduction.
- Preventing Adverse Drug Reactions
- Fatal ADRs
- Type A reactions
- Type B reactions
- Dose-related ADRs
- Allergic ADRs
- Idiosyncratic ADRs
- Drug toxicity
- Drug abuse
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Title : Mucoadhesive electrospun fibrous systems for the fast and sustained delivery of drugs
Luis Jesus Villarreal Gomez, Autonomous University of Baja California, Mexico
Title : Pharmaceutics 2023, Singapore, Abstract Pathology and Patient Safety: The Vital Role of Electronic Medical Record and Pathology Informatics in Error Reduction and Precision Medicine
Consolato M Sergi, University of Ottawa, Canada
Title : Values based practice and the impact on Drug discovery, regulation of the Pharma industry and consent in healthcare”
Ashok Handa, Collaborating Centre for Values Based Practice, United Kingdom