The DOI matches its Crossref record; 60 of the 60 references it cites were found in a registry or an index.
Apixaban: A Clinical Pharmacokinetic and Pharmacodynamic Review
Open accessAbstract
Apixaban is an oral, direct factor Xa inhibitor that inhibits both free and clot-bound factor Xa, and has been approved for clinical use in several thromboembolic disorders, including reduction of stroke risk in non-valvular atrial fibrillation, thromboprophylaxis following hip or knee replacement surgery, the treatment of deep vein thrombosis or pulmonary embolism, and prevention of recurrent deep vein thrombosis and pulmonary embolism. The absolute oral bioavailability of apixaban is ~ 50%. Food does not have a clinically meaningful impact on the bioavailability. Apixaban exposure increases dose proportionally for oral doses up to 10 mg. Apixaban is rapidly absorbed, with maximum concentration occurring 3-4 h after oral administration, and has a half-life of approximately 12 h. Elimination occurs via multiple pathways including metabolism, biliary excretion, and direct intestinal excretion, with approximately 27% of total apixaban clearance occurring via renal excretion. The pharmacokinetics of apixaban are consistent across a broad range of patients, and apixaban has limited clinically relevant interactions with most commonly prescribed medications, allowing for fixed dosages without the need for therapeutic drug monitoring. The pharmacodynamic effect of apixaban is closely correlated with apixaban plasma concentration. This review provides a summary of the pharmacokinetic, pharmacodynamic, biopharmaceutical, and drug-drug interaction profiles of apixaban. Additionally, the population-pharmacokinetic analyses of apixaban in both healthy subjects and in the target patient populations are discussed.
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Cites
Apixaban versus warfarin in patients with atrial fibrillation
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Apixaban in patients with atrial fibrillation
Connolly, S. J., Eikelboom, J., Joyner, C., Diener, H.-C., Hart, R., Golitsyn, S., Flaker, G., Avezum, A., Hohnloser, S. H., Diaz, R., et al. (2011) · New England Journal of Medicine · doi:10.1056/nejmoa1007432 · Cited by 2,483
Oral Apixaban for the Treatment of Acute Venous Thromboembolism
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Apixaban for Extended Treatment of Venous Thromboembolism
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Andexanet Alfa for the Reversal of Factor Xa Inhibitor Activity
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Antithrombotic Therapy for Atrial Fibrillation
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Andexanet Alfa for Acute Major Bleeding Associated with Factor Xa Inhibitors
Connolly, S. J., Milling, T. J., Eikelboom, J. W., Gibson, C. M., Curnutte, J. T., Gold, A., Bronson, M. D., Lu, G., Conley, P. B., Verhamme, P., et al. (2016) · New England Journal of Medicine · doi:10.1056/nejmoa1607887 · Cited by 807
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Apixaban versus Enoxaparin for Thromboprophylaxis after Hip Replacement
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Zhang, Z., Shen, W. X., Liu, Q., & Zitnik, M. (2024) · Nature Machine Intelligence · doi:10.1038/s42256-024-00920-9 · Cited by 32
Metadata
- Authors
- Byon, W., Garonzik, S., Boyd, R. A., & Frost, C. E.
- Venue
- Clinical Pharmacokinetics
- Published
- 2019-05-14
- Volume
- 58
- Issue
- 10
- Pages
- 1265-1279
- ISSN
- 0312-5963 (ISSN-L)
- 1179-1926
- OpenAlex
- W2946652117
- Cited by
- 348
- References
- 60
- FWCI
- 23.52
- Type
- journal article
- Language
- en
- Open access
- hybrid
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- Byon, W., Garonzik, S., Boyd, R. A., & Frost, C. E. (2019). Apixaban: A Clinical Pharmacokinetic and Pharmacodynamic Review. Clinical Pharmacokinetics. https://doi.org/10.1007/s40262-019-00775-z
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