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Drug ReportsGadofosveset
Ablavar, Ablavar (previously vasovist)(gadofosveset)
Ablavar, Vasovist (gadofosveset) is a small molecule pharmaceutical. Gadofosveset was first approved as Ablavar (previously vasovist) on 2005-10-03. It has been approved in Europe to treat magnetic resonance angiography.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
diagnosisD003933
Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Gadofosveset trisodium
Tradename
Company
Number
Date
Products
ABLAVARLantheus Medical ImagingN-021711 DISCN2008-12-22
2 products
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Labels
FDA
EMA
Brand Name
Status
Last Update
vasovist2009-01-02
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
V: Various drug classes in atc
V08: Contrast media
V08C: Magnetic resonance imaging contrast media
V08CA: Paramagnetic contrast media
V08CA11: Gadofosveset
HCPCS
Code
Description
A9583
Injection, gadofosveset trisodium, 1 ml
Clinical
No data
Drug
General
Drug common nameGadofosveset
INNgadofosveset
Description
Gadofosveset (trade names Vasovist, Ablavar) is a gadolinium-based MRI contrast agent. It was used as the trisodium salt monohydrate form. It acts as a blood pool agent by binding to human serum albumin. The manufacturer (Lantheus Medical) discontinued production in 2017 due to poor sales.
Classification
Small molecule
Drug classphosphoro-derivatives; gadolinium derivatives (principally for diagnostic use)
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Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID193901-90-5
RxCUI
ChEMBL IDCHEMBL1908843
ChEBI ID
PubChem CID11672461
DrugBankDB06705
UNII ID9430ZR8ZAN (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
No data
Safety
Black-box Warning
Black-box warning for: Vasovist
Adverse Events
0 adverse events reported
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