Prevalent-New User Design for Biosimilar Safety Using Saudi Real-World Data.
Almadani O; Alfakhri A; Asiri I; Alturaiki A; Alrashid A; Althunian T · 2026 · Pharmacoepidemiology and drug safety
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
The study found no significant effect — useful as a negative control or null benchmark for your own design.
Abstract (excerpt)
Objective Incidents of infections associated with biosimilar biological disease-modifying antirheumatic drugs (bDMARDs) have been communicated to the Saudi Food and Drug Authority (SFDA). This study aimed to evaluate the infection risk…
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Metadata source: Europe PMC · DOI 10.1002/pds.70388