Clinical characteristics and outcomes of venous thromboembolism (VTE) patients with concomitant anemia are unclear. This study compares baseline characteristics, treatment patterns, and 24-month outcomes in patients with and without anemia within GARFIELD-VTE. Materials and methods: GARFIELD-VTE (ClinicalTrials.gov: NCT02155491) is a global, prospective, noninterventional registry of real-world treatment practices. Of the 10,679 patients enrolled in GARFIELD-VTE, 7698 were eligible for analysis. Primary outcomes were all-cause mortality, recurrent VTE, and major bleeding in VTE patients with or without concomitant anemia over 24-months after diagnosis. Event rates and 95% confidence intervals were estimated using Poisson regression. Adjusted hazard ratios were calculated using Cox proportional hazard models. Results: Distribution of VTE events in 2771 patients with anemia and 4927 without anemia was similar (deepvein thrombosis alone: 61⋅1% vs. 55⋅9%, pulmonary embolism ± deep vein thrombosis: 38⋅9% vs. 44⋅0%, respectively). Patients with anemia were older (62.6 year vs. 58.9 years) than those without. At baseline, VTE risk factors that were more common in patients with anemia included hospitalization (22⋅0% vs. 6⋅8%), surgery (19⋅2% vs. 8⋅2%), cancer (20⋅1% vs. 5⋅6%) and acute medical illness (8⋅3% vs. 4⋅2%). Patients with anemia were more likely to receive parenteral anticoagulation therapy alone than those without anemia (26⋅6% vs. 11⋅7%) and less likely to receive a direct oral anticoagulant (38⋅5% vs. 53⋅5%). During 24-months of follow-up, patients with anemia had a higher risk (adjusted hazard ratio [95% confidence interval]) of all-cause mortality (1⋅84 [1⋅56-2⋅18]), major bleeding (2⋅83 [2⋅14-3⋅75]). Among anemia patients, the risk of all-cause mortality and major bleeding remained higher in patients with severe anemia than in those with mild/moderate anemia, allcause mortality: HR 1⋅43 [95% CI: 1⋅21-1⋅77]; major bleeding: HR 2⋅08 [95% CI: 1⋅52-2⋅86]).