# Fatal Suicide Attempt with Upadacitinib (Rinvoq®) in an Adolescent: A Case Report

**Authors:** Silviya Stoykova, Ivo Ivanov, Evgeniya Byrzashka, Vasil Atanasov

PMC · DOI: 10.3390/reports9010009 · Reports - Clinical Practice and Surgical Cases · 2025-12-24

## TL;DR

A 13-year-old girl died after overdosing on upadacitinib, showing severe health effects and highlighting the drug's fatal potential in overdose.

## Contribution

First reported case of a fatal upadacitinib overdose with lethal concentration data in humans.

## Key findings

- Upadacitinib overdose caused profound CNS depression, cardiovascular collapse, and metabolic acidosis.
- Lethal blood concentration of upadacitinib was 1.84 µg/mL, far exceeding therapeutic levels.
- Toxicity was electrophysiological and hemodynamic, not due to myocardial infarction.

## Abstract

Background and Clinical Significance: Upadacitinib, a selective Janus kinase 1 (JAK1) inhibitor, is increasingly prescribed for autoimmune and inflammatory diseases. Although its therapeutic safety profile is well established, fatal intoxications have not been reported to date. Case Presentation: We describe the first fatal case of upadacitinib overdose in a 13-year-old girl. Following ingestion of approximately 600 mg (40 × 15 mg tablets Rinvoq®), the patient presented with deep coma, profound bradycardia (~40 bpm) with third-degree atrioventricular block, conduction delay, hypotension, hypothermia, and metabolic acidosis. Laboratory tests showed hyperglycemia (17.8 mmol/L) and only minimal elevations in cardiac biomarkers (CK 57.03 U/L, CK-MB 30.64 U/L, troponin 0.003 ng/mL). Despite advanced resuscitation, the patient succumbed within a few hours. Forensic toxicology revealed extremely high concentrations of upadacitinib, 1.84 µg/mL (~1840 ng/mL) in blood and 70.3 µg/mL in gastric contents, far exceeding reported therapeutic plasma levels (Cmax 36.0 ± 8.8 ng/mL). This case establishes the first reported value for a lethal upadacitinib concentration in humans. The combination of conduction abnormalities, refractory shock, and minimal biomarker changes is consistent with an acute electrophysiological and hemodynamic collapse rather than myocardial infarction. Conclusions: The toxicity of upadacitinib in this case is characterized by profound central nervous system depression, severe cardiovascular (electrophysiological and hemodynamic) disturbances, and metabolic abnormalities (acidosis and hyperglycemia). These findings provide essential reference data for clinical and forensic toxicology, highlight the fatal potential of upadacitinib in overdose, and underscore the importance of secure medication storage and pharmacovigilance in households with adolescents.

## Linked entities

- **Proteins:** CHKA (choline kinase alpha), ckmb (creatine kinase, muscle b), LOC115584584 (troponin C, skeletal muscle)
- **Chemicals:** upadacitinib (PubChem CID 58557659), Rinvoq® (PubChem CID 58557659)

## Full-text entities

- **Genes:** JAK1 (Janus kinase 1) [NCBI Gene 3716] {aka AIIDE, JAK1A, JAK1B, JTK3}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}
- **Diseases:** overdose (MESH:D062787), bradycardia (MESH:D001919), disturbances (MESH:D014832), myocardial infarction (MESH:D009203), shock (MESH:D012769), metabolic abnormalities (MESH:D008659), hypothermia (MESH:D007035), central nervous system depression (MESH:D016543), cardiovascular ( (MESH:D002318), coma (MESH:D003128), atrioventricular block (MESH:D054537), acidosis (MESH:D000138), toxicity (MESH:D064420), hypotension (MESH:D007022), autoimmune and inflammatory diseases (MESH:D001327), conduction delay (MESH:D000074021), hyperglycemia (MESH:D006943)
- **Chemicals:** Rinvoq (MESH:C000613732)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12821496/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12821496/full.md

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Source: https://tomesphere.com/paper/PMC12821496