WHO database finds cannabis signal in rare cerebral vessel events

Drug-associated central nervous system vasculitis and reversible cerebral vasoconstriction syndrome: A global disproportionality analysis of the WHO pharmacovigilance database (VigiBase).

British journal of clinical pharmacology • • Relevant
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AI Summary

This observational case-non-case study examined medicines reported in the WHO’s VigiBase database in connection with central nervous system vasculitis (CNSV) and reversible cerebral vasoconstriction syndrome (RCVS). Researchers identified 735 CNSV cases and 1,553 RCVS cases, then compared reporting patterns while accounting for age, sex, region, and reporting characteristics. CNSV reports were most associated with immune checkpoint inhibitors and the antithyroid drug propylthiouracil, whereas RCVS reports were linked mainly to serotonergic and vasoactive drugs—including triptans, ergot derivatives, SSRIs, and cannabis.

The two conditions showed different reported timing patterns: CNSV had a median onset of 35.50 days, compared with 8.75 days for RCVS. The analysis also found a strong, newly identified RCVS reporting signal for teprotumumab, based on 6 cases, and reported that female sex was independently associated with RCVS. For cannabis, the abstract supports an association in pharmacovigilance reports, but it does not establish that cannabis caused RCVS, quantify individual risk, or show that cannabis is more hazardous than the other substances studied. This is an abstract-based summary; the database design cannot establish causation or incidence, and the abstract does not provide cannabis-specific case details.

💡 Key Findings

1
The WHO database contained 1,553 RCVS cases, with reports primarily associated with serotonergic and vasoactive agents, including cannabis.
Good
75%
2
RCVS had a shorter reported median time to onset than CNSV: 8.75 days versus 35.50 days.
High
80%
3
A novel and strong RCVS reporting signal was identified for teprotumumab, based on 6 cases and an adjusted reporting odds ratio of 60.17.
High
80%
4
Female sex was independently associated with RCVS, with an adjusted reporting odds ratio of 2.57.
High
80%

📄 Original Abstract

AIMS: This study aimed to identify and characterize drugs disproportionately associated with central nervous system vasculitis (CNSV) and reversible cerebral vasoconstriction syndrome (RCVS) in VigiBase, the World Health Organization (WHO) global pharmacovigilance database, and to describe their pharmacological and temporal profiles. METHODS: We conducted a case-non-case study in VigiBase, the WHO global pharmacovigilance database (extract June 2025). Both unadjusted and adjusted reporting odds ratios (aROR) were estimated, the latter using multivariate logistic regression accounting for age, sex, geographic region and reporting characteristics. Time-to-onset, dechallenge outcomes and fatality rates were also analysed. RESULTS: We identified 735 CNSV cases and 1553 RCVS cases. CNSV was predominantly associated with immune checkpoint inhibitors (pembrolizumab and nivolumab) and antithyroid drugs (propylthiouracil), with a median time-to-onset of 35.50 days (interquartile range [IQR] 7.75-123.25). RCVS was primarily associated with serotonergic and vasoactive agents (triptans, ergot derivatives, selective serotonin reuptake inhibitors [SSRIs] and cannabis), with a markedly shorter onset of 8.75 days (IQR 3.25-52.88). The strongest RCVS signal was a novel association with teprotumumab, an insulin-like growth factor-1 receptor (IGF-1R) inhibitor approved for thyroid eye disease (6 cases; aROR 60.17, 95% confidence interval [CI] 18.66-194.05). Female sex was independently associated with RCVS (aROR 2.57, 95% CI 2.23-2.97). CONCLUSIONS: Drug-associated CNSV and RCVS exhibit distinct pharmacological and temporal profiles, which may help inform drug withdrawal decisions and optimal management of these neurovascular emergencies.

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