Pentosan polysulfate sodium 100mg/1ml solution for injection vials
Requires a prescription from a doctor or prescriber
Pentosan polysulfate is a sulfated pentosyl polysaccharide with heparin-like properties.
Official documents, adverse reaction reporting, and safety monitoring
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Official medicine documents
Safety monitoring data
Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
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Suspected adverse reactions reported for Pentosan polysulfate sodium
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Report a side effect
Submit a Yellow Card report to the MHRA
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.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
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Suspected adverse reactions reported for Pentosan polysulfate sodium
About EudraVigilance
Learn about EU pharmacovigilance and safety monitoring
EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
1 branded products available
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(1)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
Check stock at pharmacies and supply information
Pharmacy stock checkers
Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
Supply & safety information
Official UK regulator monitoring and safety alerts
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
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: 9 · Randomised trials: 3 · 1990–2026
Showing the 50 most relevant studies, sorted by most relevant.
Lee J, Kim YJ, Lee K, et al.
2025
Mohiuddin M, Park R, Wesselmann U, et al.
2025
Clinical disorders associated with chronic pelvic pain (CPP) cause demonstrable emotional and physical dysfunction as well as increased health care utilization. Interventions that have been studied for the treatment of CPP often provide inadequate relief and/or intolerable adverse effects. The common practice of combining multiple CPP treatments needs more supportive evidence, and emerging combination trials have been evaluated in this systematic review. We searched MEDLINE and EMBASE and CENTRAL databases for CPP combination trials. This review included double-blind randomized controlled trials comparing combinations of 2 or more agents to at least 1 monotherapy in adults with CPP. The primary outcome was reduction in pain intensity or pain relief, and secondary outcomes included adverse events, quality of life, and other symptoms. Risk of bias was assessed. Nine studies (1,299 participants) were included and involved various different treatments including ciprofloxacin, tamsulosin, pentosan polysulfate, hyaluronic acid, chondroitin, hydroxyzine, troxerutin, carbazochrome, linzagolix, and allopurinol. Studies were heterogenous according to several features including studied treatments, dose and route of administration, and underlying condition such that no studies could be combined for meta-analysis. None of the included studies reported a significant difference in reducing pain intensity for combination therapy vs monotherapy. If future proof-of-concept studies demonstrate that a given combination is superior to all monotherapy components, subsequent large, double-blind randomized, controlled clinical trials of such combinations for CPP are required to better elucidate the role of combination therapy in clinical settings.
Abstract licence: CC BY-NC-ND
Edward L Davis, Samar R. El Khoudary, E. Talbott, et al.
The Journal of urology, 2008
- Cystitis, Interstitial
- Pentosan Sulfuric Polyester
- Administration, Intravesical
Donna L. Skerrett, Catherine J. M. Stapledon, Mukesh Ahuja, et al.
Arthritis Research & Therapy, 2026
- Synovial Fluid
- Osteoarthritis, Knee
- Pentosan Sulfuric Polyester
William A. Pearce, Rui Chen, Nieraj Jain
Ophthalmology, 2018
- Dyslexia
- Vision Disorders
- Retinitis Pigmentosa
S. Mulholland, G. Sant, P. Hanno, et al.
Urology, 1990
J. Nickel, J. Barkin, J. Forrest, et al.
Urology, 2005
- Cystitis, Interstitial
- Pentosan Sulfuric Polyester
- Anti-Inflammatory Agents, Non-Steroidal
Chi-Shin Tseng, Shang-Jen Chang, En Meng, et al.
Journal of the Formosan Medical Association, 2020
J. Sairanen, T. Tammela, M. Leppilahti, et al.
The Journal of urology, 2005
- Syncope
- Cystitis, Interstitial
- Cyclosporine
Ahmad Santina, Alessandro Feo, Elodie Bousquet, et al.
Survey of ophthalmology, 2024
- Macula Lutea
- Inflammatory Bowel Diseases
- Retinal Diseases
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
154 found
Half-life
4.8 hours
Mechanism
Pentosan polysulfate is a polymer of xylose hydrogen sulfate and contains two sulfate groups per carbohydrate monomer.
Food interactions
2 warnings
Human targets
3 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
Half-life
4.8 hours
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 713 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
Proteins and enzymes this drug interacts with in the body
PMID:8663044
Also acts as an integrin ligand which is required for FGF2 signaling .
PMID:28302677
Binds to integrin ITGAV:ITGB3 .
PMID:28302677
Plays an important role in the regulation of cell survival, cell division, cell differentiation and cell migration .
PMID:28302677 PMID:8663044
Functions as a potent mitogen in vitro .
PMID:1721615 PMID:3732516 PMID:3964259
Can induce angiogenesis .
PMID:23469107 PMID:28302677
Mediates phosphorylation of ERK1/2 and thereby promotes retinal lens fiber differentiation PMID:29501879
Binds to FGFR1 in the presence of heparin leading to FGFR1 dimerization and activation via sequential autophosphorylation on tyrosine residues which act as docking sites for interacting proteins, leading to the activation of several signaling cascades. Binds to integrin ITGAV:ITGB3. Its binding to integrin, subsequent ternary complex formation with integrin and FGFR1, and the recruitment of PTPN11 to the complex are essential for FGF1 signaling.
Induces the phosphorylation and activation of FGFR1, FRS2, MAPK3/ERK1, MAPK1/ERK2 and AKT1 .
PMID:18441324 PMID:20422052
Can induce angiogenesis PMID:23469107
ATC C05BA51
ATC C05BA04
ATC G04BX15
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)
Additional database identifiers
Drugs Product Database (DPD)
716
ChemSpider
34595
ZINC
ZINC000014879975
HUGO Gene Nomenclature Committee (HGNC)
HGNC:3676
GenAtlas
FGF2
GeneCards
FGF2
GenBank Gene Database
X04431
GenBank Protein Database
31362
UniProt Accession
FGF2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:3665
GenAtlas
FGF1
GeneCards
FGF1
GenBank Gene Database
M13361
GenBank Protein Database
181942
UniProt Accession
FGF1_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:3682
GenAtlas
FGF4
GeneCards
FGF4
GenBank Gene Database
J02986
GenBank Protein Database
386788
UniProt Accession
FGF4_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite the following publications:
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Structured knowledge from the free knowledge base
Linked open data from Wikidata (Q7165276), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.