Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Floxuridine
Drug ID BADD_D00908
Description An antineoplastic antimetabolite that is metabolized to fluorouracil when administered by rapid injection. Floxuridine is available as a sterile, nonpyrogenic, lyophilized powder for reconstitution. When administered by slow, continuous, intra-arterial infusion, it is converted to floxuridine monophosphate. It has been used to treat hepatic metastases of gastrointestinal adenocarcinomas and for palliation in malignant neoplasms of the liver and gastrointestinal tract.
Indications and Usage For palliative management of gastrointestinal adenocarcinoma metastatic to the liver, when given by continuous regional intra-arterial infusion in carefully selected patients who are considered incurable by surgery or other means. Also for the palliative management of liver cancer (usually administered by hepatic intra-arterial infusion).
Marketing Status approved
ATC Code L01BC09
DrugBank ID DB00322
KEGG ID D04197
MeSH ID D005467
PubChem ID 5790
TTD Drug ID D0TS1Z
NDC Product Code 63323-145; 0143-9270; 81643-9270; 59605-5352
UNII 039LU44I5M
Synonyms Floxuridine | 5-FUdR | FUdR | Fluorodeoxyuridine | 5-Fluorodeoxyuridine | 5 Fluorodeoxyuridine
Chemical Information
Molecular Formula C9H11FN2O5
CAS Registry Number 50-91-9
SMILES C1C(C(OC1N2C=C(C(=O)NC2=O)F)CO)O
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Rash maculo-papular23.03.13.004--
Skin fissures23.03.03.008--Not Available
Skin hyperpigmentation23.05.01.003--
Stomatitis07.05.06.005--
Thrombocytopenia01.08.01.002--Not Available
Thrombophlebitis24.01.02.001--Not Available
Vein discolouration24.03.02.004--Not Available
Vomiting07.01.07.003--
Fibromyalgia15.05.02.002--Not Available
Red blood cell sedimentation rate abnormal13.01.03.004--Not Available
Onychomadesis23.02.05.006--
Catheter site haemorrhage12.07.02.002; 08.02.02.002; 24.07.01.003--Not Available
Dacryostenosis acquired06.06.04.003--Not Available
Transaminases increased13.03.04.036--Not Available
Haemorrhage24.07.01.002--Not Available
Catheter site infection12.07.02.006; 11.01.08.022; 08.02.02.006--Not Available
Procedural complication12.02.05.005--
Skin toxicity23.03.03.032; 12.03.01.020--Not Available
Blood alkaline phosphatase increased13.04.02.004--
Biliary tract disorder09.02.03.001--Not Available
Embolism24.01.01.009--
Ischaemia24.04.02.004--Not Available
Decreased appetite14.03.01.005; 08.01.09.028--
Ill-defined disorder08.01.03.049--Not Available
Device occlusion27.01.02.003--Not Available
Catheter site extravasation12.07.02.012; 08.02.02.012--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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