A Two-Year Pharmacovigilance Analysis of Adverse Drug Reactions Reported from a University Allergy Setting
Paola Maria Cutroneo, Ilaria Marando, Stefania Isola, Angela Alibrandi, Marco Casciaro, Paola Lucia Minciullo, Edoardo Spina, Sebastiano Gangemi, Luisa Ricciardi

TL;DR
This study analyzed 388 adverse drug reaction reports from an allergy clinic over two years to identify risk factors and patterns.
Contribution
The study reveals that a history of allergies or past ADRs is linked to fewer serious ADRs, likely due to heightened awareness.
Findings
Most ADRs were immediate, from antibiotics and anti-inflammatories, with skin and respiratory issues being common.
Elderly patients (≥65 years) had a higher risk of serious ADRs.
Anaphylactic shock was rare, occurring in only 3.35% of reports.
Abstract
Background: Adverse Drug Reactions (ADRs) are a significant public concern because of their impact on healthcare systems. Spontaneous reporting of ADRs is crucial for monitoring drug safety and recognizing possible risk factors. The objective of this study was to characterize ADR reports from the Allergy and Clinical Immunology Unit of the G. Martino University Hospital, Messina, Italy. Methods: A retrospective analysis was conducted, including all ADRs spontaneously reported from patients attending the clinic because of at least one previous ADR, from June 2022 to June 2024. Results: A total of 388 reports were collected, mainly from females (71.1%) and adult patients (84.3%). ADRs were mostly immediate, from antibiotics and anti-inflammatory drugs (61.5%), with a high prevalence of cutaneous and respiratory disorders. Delayed reactions were mostly from endocrine therapies, vaccines,…
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Taxonomy
TopicsPharmacovigilance and Adverse Drug Reactions · Drug-Induced Adverse Reactions · Biosimilars and Bioanalytical Methods
