Zoledronic acid 4mg/5ml solution for infusion vials
Requires a prescription from a doctor or prescriber
Drugs affecting bone metabolism
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 Zoledronic acid
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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 Zoledronic acid
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EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
18 branded products available
MHRA licensed products
View all licensed products for Zoledronic acid on the MHRA register
Zometa 4mg/5ml solution for infusion vials
Zoledronic acid 4mg/5ml concentrate for solution for infusion vials
Zoledronic acid 4mg/5ml concentrate for solution for infusion vials
Zoledronic acid 4mg/5ml concentrate for solution for infusion vials
Zoledronic acid 4mg/5ml concentrate for solution for infusion vials
Zoledronic acid 4mg/5ml concentrate for solution for infusion vials
Zoledronic acid 4mg/5ml concentrate for solution for infusion vials
Zoledronic acid 4mg/5ml concentrate for solution for infusion vials
Zoledronic acid 4mg/5ml concentrate for solution for infusion vials
Sun Pharmaceutical Industries Europe B.V.
Zoledronic acid 4mg/5ml concentrate for solution for infusion vials
WHO defined daily dose (DDD)
4 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 NHS dm+d BNF mapping files. Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity based on WHO Anatomical Therapeutic Chemical (ATC) classification and NHS BNF section grouping. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Clinical guidelines and formulary information
British National Formulary
Zoledronic acid
Source: British National Formulary, NICE. Joint Formulary Committee. Contains public sector information licensed under the Open Government Licence v3.0.
NICE clinical guidance(7)
Myeloma: diagnosis and management (NG35)
Denosumab for the prevention of skeletal-related events in adults with bone metastases from solid tumours (TA265)
Osteoporosis (QS149)
Bisphosphonates for treating osteoporosis (TA464)
Prostate cancer: diagnosis and management (NG131)
Romosozumab for treating severe osteoporosis (TA791)
Early and locally advanced breast cancer: diagnosis and management (NG101)
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 & product information
Official product databases and supply status monitoring
Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. emc (electronic medicines compendium) is operated by Datapharm Ltd. Shortage information sourced from NHS Specialist Pharmacy Service (SPS), sps.nhs.uk.
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF codes from NHS Business Services Authority (NHSBSA). 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.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
107 found
Half-life
146 hours
Mechanism
Bisphosphonates are taken into the bone where they bind to hydroxyapatite.
Food interactions
None known
Human targets
3 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
4mg
Half-life
146 hours
[L13712][L13715][L13721]
Protein binding
23-53%
[L13712][L13715][L13721]
Metabolism
[L13712][L13715][L13721]
Elimination
16%
[L13712][L13715][L13721]
Clearance
2.0 L/h
[L13712][L13715][L13721]
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Zoledronic acid was granted FDA approval on 20 August 2001.[L13712]
[L13712][L13715][L13721]
Zoledronic acid is also indicated for the prevention of osteoporosis in post menopausal women and glucocorticoid induced osteoporosis.
[L13712][L13715][L13721]
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 316 interactions
[L13712][L13715][L13721]
Overdose should be managed through intravenous administration of the insufficient ions.
[L13712][L13715][L13721]
Osteoclasts mediate resorption of bone.[A6366] When osteoclasts bind to bone they form podosomes, ring structures of F-actin.[A6366] Etidronic acid also inhibits V-ATPases in the osteoclast, though the exact subunits are unknown, preventing F-actin from forming podosomes.[A202229][A202247][A203360] Disruption of the podosomes causes osteoclasts to detach from bones, preventing bone resorption.[A6366]
Nitrogen containing bisphosphonates such as zoledronate are known to induce apoptosis of hematopoietic tumor cells by inhibiting the components of the mevalonate pathway farnesyl diphosphate synthase, farnesyl diphosphate, and geranylgeranyl diphosphate.[A202769][A203123] These components are essential for post-translational prenylation of GTP-binding proteins like Rap1.[A202769][A203123] The lack of prenylation of these proteins interferes with their function, and in the case of Rap1, leads to apoptosis.[A202769][A203123] zoledronate also activated caspases which further contribute to apoptosis.[A202769][A203123]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[A203099]
A 5mg intravenous dose reaches a Cmax of 471±76.1ng/mL, with a Tmax of 0.368±0.005h, and an AUC of 917±226ng\*h/mL.
[A203099]
[L13712][L13715][L13721]
[L13712][L13715][L13721]
[L13712][L13715][L13721]
[L13712][L13715][L13721]
[L13712][L13715][L13721]
Proteins and enzymes this drug interacts with in the body
Proteins that transport this drug across cell membranes
PMID:10064732 PMID:11114332 PMID:16230346 PMID:7961706 PMID:9281595
Mediates ATP-dependent transport of glutathione and glutathione conjugates, leukotriene C4, estradiol-17-beta-o-glucuronide, methotrexate, antiviral drugs and other xenobiotics .
PMID:10064732 PMID:11114332 PMID:16230346 PMID:7961706 PMID:9281595
Confers resistance to anticancer drugs by decreasing accumulation of drug in cells, and by mediating ATP- and GSH-dependent drug export .
PMID:9281595
Hydrolyzes ATP with low efficiency .
PMID:16230346
Catalyzes the export of sphingosine 1-phosphate from mast cells independently of their degranulation .
PMID:17050692
Participates in inflammatory response by allowing export of leukotriene C4 from leukotriene C4-synthesizing cells (By similarity). Mediates ATP-dependent, GSH-independent cyclic GMP-AMP (cGAMP) export .
PMID:36070769
Thus, by limiting intracellular cGAMP concentrations negatively regulates the cGAS-STING pathway .
PMID:36070769
Exports S-geranylgeranyl-glutathione (GGG) in lymphoid cells and stromal compartments of lymphoid organs. ABCC1 (via extracellular transport) with GGT5 (via GGG catabolism) establish GGG gradients within lymphoid tissues to position P2RY8-positive lymphocytes at germinal centers in lymphoid follicles and restrict their chemotactic transmigration from blood vessels to the bone marrow parenchyma (By similarity).
Mediates basolateral export of GSH-conjugated R- and S-prostaglandin A2 diastereomers in polarized epithelial cells PMID:9426231
ATC M05BB08
ATC M05BA08
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)
Zoledronic acid
Additional database identifiers
Drugs Product Database (DPD)
12024
ChemSpider
61986
BindingDB
12578
PDB
ZOL
ZINC
ZINC000003803652
HUGO Gene Nomenclature Committee (HGNC)
HGNC:4249
GeneCards
GGPS1
GenBank Gene Database
AB017971
GenBank Protein Database
4520350
Guide to Pharmacology
643
UniProt Accession
GGPPS_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:3631
GenAtlas
FDPS
GeneCards
FDPS
GenBank Gene Database
J05262
GenBank Protein Database
182399
Guide to Pharmacology
644
UniProt Accession
FPPS_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:51
GenAtlas
ABCC1
GeneCards
ABCC1
GenBank Gene Database
L05628
GenBank Protein Database
1835659
Guide to Pharmacology
779
UniProt Accession
MRP1_HUMAN
International reference pricing
Reference pricing from DrugBank. Prices are indicative and may not reflect current UK costs.
Source: DrugBank. Used under CC BY-NC 4.0 academic licence for non-commercial purposes.
Patent information
1 active patent, 5 expired
Source: DrugBank · CC BY-NC 4.0. Patent data sourced from national patent offices. Expiry dates may not reflect extensions, regulatory exclusivity periods, or legal challenges.
DrugBank citations
If you use DrugBank data in your research, please cite the following publications: