Rasburicase 1.5mg powder and solvent for solution for infusion vials
Requires a prescription from a doctor or prescriber
Rasburicase is a recombinant urate-oxidase enzyme produced by a genetically modified <i>Saccharomyces cerevisiae</i> strain.
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Yellow Card reports
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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Fasturtec 1.5mg powder and solvent for solution for infusion vials
WHO defined daily dose (DDD)
14 mg
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 15 · Randomised trials: 1 · 2011–2026
Showing the 50 most relevant studies, sorted by most relevant.
Revania Radina Thirza, Denaya Khansa
Indonesian Journal of Biomedicine and Clinical Sciences, 2025
S. Kumar, A. Meeter, R. Patel, et al.
American Journal of Respiratory and Critical Care Medicine, 2026
B. Vidhyashree, M. Zuber, Shifa Taj, et al.
Journal of Oncology Pharmacy Practice, 2021
Li QH, Mo YQ, Zeng WC, et al.
2023
- Gout
- Arthritis, Gouty
- Uric Acid
N. Alakel, J. Middeke, J. Schetelig, et al.
OncoTargets and therapy, 2017
M. Hammami, Asma Qasim, R. Thakur, et al.
Annals of Hematology, 2023
- Anemia, Hemolytic
- Methemoglobinemia
- Tumor Lysis Syndrome
Papapanou M, Athanasopoulos AE, Georgiadi E, et al.
2023
- Lung Neoplasms
- Tumor Lysis Syndrome
- Acute Kidney Injury
No systematic synthesis of all cases of spontaneous tumor lysis syndrome (STLS) in adult patients with solid tumors is available to date. Herein, we aim to recognize specific STLS characteristics and parameters related to a worse prognosis. We conducted a systematic search for randomized controlled trials, cohorts, case-control studies, and case reports. The primary endpoints were death and the need for renal replacement therapy (RRT) due to STLS. We estimated crude odds ratios (ORs) with 95% confidence intervals (95%CI) via univariate binary logistic regression. We included one cohort of 9 patients and 66 case reports of 71 patients [lung cancer 15(21.1%)]. Regarding the case reports, most patients [61(87.1%)] had metastatic disease [liver 46(75.4%)], developed acute kidney injury [59(83.1%)], needed RRT [25(37.3%)], and died due to STLS [36(55.4%)]. Metastatic disease, especially in the liver [p = 0.035; OR (95%CI): 9.88 (1.09, 89.29)] or lungs [p = 0.024; 14.00 (1.37, 142.89)], was significantly associated with STLS-related death compared to no metastasis. Cases resulting in death had a significantly higher probability of receiving rasburicase monotherapy than receiving no urate-lowering agents [p = 0.034; 5.33 (1.09, 26.61)], or the allopurinol-rasburicase combination [p = 0.023; 7.47 (1.40, 39.84)]. Patients receiving allopurinol were less likely to need RRT compared to those not receiving it or those receiving rasburicase. In conclusion, current anecdotal evidence demonstrated that metastatic disease, especially in the liver and lungs, may be associated with STLS-related death compared to no metastatic status. Careful surveillance of high-risk cases within larger studies is essential to identify markers predicting morbidity or mortality.
Abstract licence: CC BY
Kamran Mahfooz, Haris Sohail, A. Gvajaia, et al.
Cancer Pathogenesis and Therapy, 2023
Anselm Chi-wai Lee
Hematology Reports, 2025
Siddiqui Z, Schab AR, Paracha A, et al.
2026
- Lung Neoplasms
- Tumor Lysis Syndrome
- Uric Acid
BackgroundTumor lysis syndrome (TLS) in patients with lung cancer (LC) is poorly characterized, due to its predominance in hematologic malignancies, creating a gap in both recognition and management strategies.MethodsWe reviewed the literature to identify features that distinguish patients with lung cancer (LC) at high risk for tumor lysis syndrome (TLS) and poor prognosis, and to evaluate treatment outcomes. The PubMed database was queried through February 2025 in accordance with PRISMA guidelines. Twenty-nine case reports, including clinical courses and biochemical data of LC patients who developed TLS, were analyzed and appraised.ResultsRisk factors for tumor lysis syndrome (TLS) included elevated uric acid and lactate dehydrogenase (LDH) at baseline, along with dyspnea, oliguria, and lethargy. Factors associated with increased mortality included high baseline LDH, symptomatic TLS, the need for renal replacement therapy, liver metastasis, and widespread metastatic disease. Rasburicase was associated with improved survival in a limited subset. Mortality in patients with lung cancer (LC) and TLS rivaled that observed in hematologic malignancies.ConclusionFor patients with high-risk lung cancer (LC), proactive initiation of urate-lowering therapy and hydration along with rasburicase and continued hydration for those who develop tumor lysis syndrome (TLS) may reduce mortality. Further multicenter studies may influence diagnostic criteria, risk assessment, and prophylactic guidelines for TLS to better account for high-risk LC and other solid tumor patients.
Abstract licence: CC BY
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
None known
Half-life
18 hours
Mechanism
Rasburicase catalyzes enzymatic oxidation of uric acid into an inactive and soluble metabolite (allantoin).
Food interactions
None known
Human targets
1 target
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Half-life
18 hours
Volume of distribution
110 to 127 mL
* 75.8 to 138 mL/kg [adult patients]
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medicines. Always consult a healthcare professional.
Showing 50 of 53 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
* 75.8 to 138 mL/kg [adult patients]
ATC V03AF07
ATC M04AX01
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Rasburicase
DrugBank citations
If you use DrugBank data in your research, please cite:
- DrugBank 6.02024Recommended citationKnox C., Wilson M., Klinger C.M., et alDrugBank 6.0: the DrugBank Knowledgebase for 2024Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275
- DrugBank 5.02018Wishart D.S., Feunang Y.D., Guo A.C., et alDrugBank 5.0: a major update to the DrugBank database for 2018Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082
- DrugBank 4.02014Law V., Knox C., Djoumbou Y., et alDrugBank 4.0: shedding new light on drug metabolismNucleic Acids Res. 2014 Jan 142(1):D1091-7
- DrugBank 3.02011Knox C., Law V., Jewison T., et alDrugBank 3.0: a comprehensive resource for 'omics' research on drugsNucleic Acids Res. 2011 Jan39(Database issue):D1035-41
- DrugBank 2.02008Wishart D.S., Knox C., Guo A.C., et alDrugBank: a knowledgebase for drugs, drug actions and drug targets.Nucleic Acids Research2008 Jan36(Database issue):D901-6
- DrugBank 1.02006Wishart D.S., Knox C., Guo A.C., et alDrugBank: a comprehensive resource for in silico drug discovery and exploration.Nucleic Acids Research2006 Jan 134(Database issue):D668-72