Significance of Adverse reaction
Adverse reactions refer to unintended negative effects that can occur as a result of using pharmaceutical products. These reactions can range from mild symptoms like nausea and dizziness to severe complications and require careful monitoring during treatment. Various studies highlighted different medications and treatments that may lead to such reactions, while some reported no adverse effects, indicating the safety of those treatments. Overall, monitoring for adverse reactions is crucial in the administration of medications and therapies.
Synonyms: Side effect, Negative response, Harmful effect, Adverse effect, Negative effect, Unfavorable outcome
The below excerpts are indicatory and do represent direct quotations or translations. It is your responsibility to fact check each reference.
The concept of Adverse reaction in local and regional sources
Adverse reaction denotes unintended negative effects resulting from pharmaceutical use, highlighting the potential risks associated with medication. Understanding these reactions is crucial for patient safety and effective healthcare management.
From: Triveni Journal
(1) Unintended negative effects that may occur as a result of using a pharmaceutical product.[1]
The concept of Adverse reaction in scientific sources
Adverse reaction encompasses unwanted and harmful responses to drugs or treatments, including mild cognitive disorientation noted in a study, with no serious side effects reported, highlighting the importance of monitoring patient experiences during medical interventions.
From: The Malaysian Journal of Medical Sciences
(1) This term refers to negative or undesirable medical events that occur after a medical intervention such as a vaccination, and these events can vary in severity and nature.[2] (2) These are undesirable effects that can occur from medical treatments, and the text mentions that serious ones associated with IVIG include hyper-viscosity syndrome and acute renal failure.[3] (3) Negative effects experienced by patients as a consequence of taking a drug, which need to be reported for safety monitoring.[4] (4) Unfavorable responses that could occur in either the infant or mother due to medical procedures.[5] (5) Unfavorable or harmful responses experienced by patients due to medication, which can lead to complications or hospitalisation.[6]