Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Vandetanib
Drug ID BADD_D02334
Description Vandetanib is an oral once-daily kinase inhibitor of tumour angiogenesis and tumour cell proliferation with the potential for use in a broad range of tumour types. On April 6 2011, vandetanib was approved by the FDA to treat nonresectable, locally advanced, or metastatic medullary thyroid cancer in adult patients.
Indications and Usage Vandetanib is currently approved as an alternative to local therapies for both unresectable and disseminated disease. Because Vandetanib can prolong the Q-T interval, it is contraindicated for use in patients with serious cardiac complications such as congenital long QT syndrome and uncompensated heart failure.
Marketing Status Prescription
ATC Code L01EX04
DrugBank ID DB05294
KEGG ID D06407
MeSH ID C452423
PubChem ID 3081361
TTD Drug ID D0G6QF
NDC Product Code 58468-7820; 49187-0220; 58468-7840
Synonyms vandetanib | N-(4-bromo-2-fluorophenyl)-6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazolin-4-amine | ZD 6474 | ZD6474 | ZD-6474 | ZD-64 | Caprelsa | Zactima
Chemical Information
Molecular Formula C22H24BrFN4O2
CAS Registry Number 443913-73-3
SMILES CN1CCC(CC1)COC2=C(C=C3C(=C2)N=CN=C3NC4=C(C=C(C=C4)Br)F)OC
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Small intestinal perforation07.04.06.006--
Stevens-Johnson syndrome23.03.01.007; 12.03.01.014; 11.07.01.005; 10.01.03.020--
Stomatitis07.05.06.005--
Sudden death08.04.01.003; 02.03.04.013--
Syncope24.06.02.012; 17.02.04.008; 02.01.02.0080.000533%
Thrombocytopenia01.08.01.002--Not Available
Torsade de pointes02.03.04.005--Not Available
Tracheitis22.07.03.009; 11.01.13.007--
Transient ischaemic attack24.04.06.005; 17.08.04.001--
Tremor17.01.06.0020.000533%
Tuberculosis11.04.01.0060.000533%Not Available
Upper respiratory tract infection22.07.03.011; 11.01.13.009--
Urethral disorder20.07.01.002--Not Available
Urinary tract disorder20.08.01.001--Not Available
Urinary tract infection20.08.02.001; 11.01.14.004--
Vena cava thrombosis24.01.10.001--Not Available
Ventricular arrhythmia02.03.04.006--
Vision blurred17.17.01.010; 06.02.06.0070.000533%
Visual acuity reduced06.02.03.001; 17.17.01.011--
Visual impairment06.02.06.0080.000139%Not Available
Vomiting07.01.07.003--
Weight decreased13.15.01.005--
Weight increased13.15.01.0060.000533%
White blood cell count decreased13.01.06.012--
Tubulointerstitial nephritis20.05.02.002--Not Available
Musculoskeletal disorder15.03.01.004--Not Available
Brain oedema12.01.10.010; 17.07.02.003--
General physical health deterioration08.01.03.018--Not Available
Balance disorder17.02.02.007--Not Available
Staphylococcal bacteraemia11.02.05.001--Not Available
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