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Association between selective serotonin reuptake inhibitors and upper gastrointestinal bleeding: population based
F J de Abajo1, L A Rodríguez, D Montero
1División de Farmacoepidemiología y Farmacovigilancia, Agencia Española del Medicamento, 28220 Majadahonda, Madrid, Spain. fabajo@agemed.es
Selective serotonin reuptake inhibitors (SSRIs) are associated with an increased risk of upper gastrointestinal bleeding. Combining SSRIs with NSAIDs or aspirin significantly elevates this risk, underscoring the need for careful patient management.
Area of Science:
- Pharmacovigilance
- Gastroenterology
- Clinical Epidemiology
Background:
- Selective serotonin reuptake inhibitors (SSRIs) are widely prescribed antidepressants.
- Upper gastrointestinal bleeding is a significant clinical concern with various contributing factors.
Purpose of the Study:
- To investigate the association between SSRI use and the risk of upper gastrointestinal bleeding.
- To evaluate the impact of concurrent use of SSRIs with other medications on this risk.
Main Methods:
- A population-based case-control study was conducted using data from UK general practices.
- 1651 cases of upper gastrointestinal bleeding and 10,000 controls were analyzed.
- Exposure to SSRIs and other antidepressants within 30 days of the index date was assessed.
Main Results:
- Current SSRI use was associated with a 3-fold increased risk of upper gastrointestinal bleeding (adjusted rate ratio 3.0).
- This risk was not significantly modified by patient demographics, SSRI dose, or duration of treatment.
- Concurrent use of SSRIs with non-steroidal anti-inflammatory drugs (NSAIDs) or aspirin substantially increased the risk of gastrointestinal bleeding.
Conclusions:
- SSRIs are linked to a moderate increase in upper gastrointestinal bleeding risk.
- The risk is significantly amplified when SSRIs are co-prescribed with NSAIDs or aspirin.
- Clinicians should exercise caution when prescribing SSRIs, particularly in patients also taking NSAIDs or aspirin.
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