Certoparin sodium 3,000units/0.3ml solution for injection pre-filled syringes
Certoparin is part of the heparins of low molecular weight that presents high activity against the coagulation factor Xa.
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Suspected adverse reactions reported for Certoparin
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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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1 branded products available
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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Supply & safety information
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Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary.
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: 2 · Randomised trials: 2 · 1996–2025
Showing the 50 most relevant studies, sorted by most relevant.
G. V. Tempelhoff, J. Harenberg, F. Niemann, et al.
International journal of oncology, 2000
- Breast Neoplasms
- Uterine Cervical Neoplasms
- Heparin
Grassman Ed, Fred Leya, J. Fareed, et al.
PubMed, 2001
- Angioplasty, Balloon, Coronary
- Anticoagulants
- Coronary Artery Disease
H. Diener, E. Ringelstein, R. von Kummer, et al.
Stroke: Journal of the American Heart Association, 2001
- Anticoagulants
- Brain Ischemia
- Germany
H. Diener, E. Ringelstein, R. von Kummer, et al.
Stroke, 2006
- Heparin
- Heparin, Low-Molecular-Weight
- Ischemia
Eva Wardenbach, Dino Podlesek, Boshr Alhasan, et al.
Scientific Reports, 2025
- Anticoagulants
- Brain Neoplasms
- Glioblastoma
Thromboembolic events (TE) are serious complications following glioblastoma (GBM) resection. This retrospective study analyzed 695 GBM patients (2017-2022, University Hospital Dresden) to assess the impact of different anticoagulant regimens-certoparin, enoxaparin, and enoxaparin with intermittent pneumatic stockings (IPS)-along with patient comorbidities, on TE incidence. Overall, 28 patients (4%) developed TE. The highest combined incidence of deep vein thrombosis (DVT) and pulmonary embolism (PE) occurred in the enoxaparin group (8.6%), followed by certoparin (6.9%) and enoxaparin + IPS (2.6%) (p = .003). Increased PE risk was associated with longer surgery duration (median 249 vs. 190 min; p = .002), greater intraoperative blood loss (300 vs. 150 mL; p = .002), and older age (> 65 years, p = .043). Comorbidities such as diabetes (p = .005) and coronary heart disease (p = .037) were also linked to elevated TE risk. Multivariate analysis identified enoxaparin alone as an independent risk factor (HR 0.312; CI 0.116-0.842; p = .022). Patients with PE or DVT had surgeries that were on average 45 min longer and involved higher blood loss. GBM patients treated with enoxaparin alone have a significantly higher risk for TE compared to treatment with certoparin or the combination of enoxaparin with IPS. Additionally, the duration of surgery, patient age and comorbidities significantly influence the risk of postoperative TE.
Abstract licence: CC BY 4.0
Wardenbach E, Prilop I, Benker-Hasani E, et al.
2025
Abstract Purpose This study aims to evaluate the effectiveness of different thromboprophylaxis regimens, certoparin, enoxaparin, and enoxaparin combined with intermittent pneumatic stockings (IPS), in reducing thromboembolic events (TE) after meningioma surgery, and to identify patient- and procedure-specific risk factors associated with TE. Methods A prospective cohort of 877 patients undergoing surgical resection of meningiomas was analyzed. Patients were stratified into three prophylaxis groups: certoparin, enoxaparin, and enoxaparin + IPS. Clinical variables such as age, sex, comorbidities, blood loss, surgery duration, tumor location and volume were assessed. Statistical analyses included chi-square tests and ANOVA. Results The overall incidence of TE was 3.1% (n = 27). TE rates were similar across groups: certoparin (3.5%), enoxaparin (3.5%), and enoxaparin + IPS (2.6%), with no statistically significant differences (p > .05). Chronic heart disease (p = .002) and surgery duration > 200 minutes (p = .004) were identified as independent risk factors for TE. Conclusion All three thromboprophylaxis regimens demonstrated comparable efficacy in preventing postoperative TE. Although not statistically significant, the combination of enoxaparin and IPS was associated with the lowest TE rate and no fatal events. These findings support risk-adapted prophylaxis strategies in patients with elevated procedural or cardiovascular risk.
Abstract licence: CC BY
Wardenbach E, Podlesek D, Alhasan B, et al.
2025
Abstract Thromboembolic events (TE) are serious complications following glioblastoma (GBM) resection. This retrospective study analyzed 695 GBM patients (2017–2022, University Hospital Dresden) to assess the impact of different anticoagulant regimens—certoparin, enoxaparin, and enoxaparin with intermittent pneumatic stockings (IPS)—along with patient comorbidities, on TE incidence. Overall, 28 patients (4%) developed TE. The highest combined incidence of deep vein thrombosis (DVT) and pulmonary embolism (PE) occurred in the enoxaparin group (8.6%), followed by certoparin (6.9%) and enoxaparin + IPS (2.6%) (p = .003). Increased PE risk was associated with longer surgery duration (median 249 vs. 190 min; p = .002), greater intraoperative blood loss (300 vs. 150 mL; p = .002), and older age (>65 years, p = .043). Comorbidities such as diabetes (p = .005) and coronary heart disease (p = .037) were also linked to elevated TE risk. Multivariate analysis identified enoxaparin alone as an independent risk factor (HR 0.312; CI 0.116–0.842; p = .022). Patients with PE or DVT had surgeries that were on average 45 minutes longer and involved higher blood loss. GBM patients treated with enoxaparin alone have a significant higher risk for TE compared to treatment with certoparin or the combination of enoxaparin with IPS. Additionally, the duration of surgery, patient age and comorbidities significantly influence the risk of postoperative TE.
Abstract licence: CC BY
Marco Paolo Donadini, Walter Ageno, Luigina Guasti, et al.
Expert Opinion on Drug Metabolism & Toxicology, 2013
- Clinical Trials as Topic
- Drug Evaluation
- Heparin, Low-Molecular-Weight
C. Kirchmaier, H. Wolf, H. Schäfer, et al.
International angiology : a journal of the International Union of Angiology, 1998
- Femoral Vein
- Iliac Vein
- Anticoagulants
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
1 found
Half-life
Not available
Mechanism
Not available
Food interactions
1 warning
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Known interactions with other medications. Always consult a healthcare professional.
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Chemical identifiers
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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)
Certoparin
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Structured knowledge from the free knowledge base
Linked open data from Wikidata (Q13582130), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. WHO INN from the World Health Organization.