Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Vorinostat
Drug ID BADD_D02370
Description Vorinostat (rINN) or suberoylanilide hydroxamic acid (SAHA), is a drug currently under investigation for the treatment of cutaneous T cell lymphoma (CTCL), a type of skin cancer, to be used when the disease persists, gets worse, or comes back during or after treatment with other medicines. It is the first in a new class of agents known as histone deacetylase inhibitors. A recent study suggested that vorinostat also possesses some activity against recurrent glioblastoma multiforme, resulting in a median overall survival of 5.7 months (compared to 4 - 4.4 months in earlier studies). Further brain tumor trials are planned using combinations of vorinostat with other drugs.
Indications and Usage For the treatment of cutaneous manifestations in patients with cutaneous T-cell lymphoma who have progressive, persistent or recurrent disease on or following two systemic therapies.
Marketing Status Prescription
ATC Code L01XH01
DrugBank ID DB02546
KEGG ID D06320
MeSH ID D000077337
PubChem ID 5311
TTD Drug ID D0E7PQ
NDC Product Code 0006-0568; 43744-631; 63285-009; 72969-091
Synonyms Vorinostat | N1-Hydroxy-N8-phenyloctanediamide | N1 Hydroxy N8 phenyloctanediamide | NHNPODA | Suberoyl Anilide Hydroxamic Acid | Suberoylanilide Hydroxamic Acid | N-Hydroxy-N'-phenyloctanediamide | N Hydroxy N' phenyloctanediamide | Suberanilohydroxamic Acid | M344 | MK-0683 | MK 0683 | MK0683 | 18F-SAHA | 18F-Suberoylanilide Hydroxamic Acid | 18F Suberoylanilide Hydroxamic Acid | Zolinza
Chemical Information
Molecular Formula C14H20N2O3
CAS Registry Number 149647-78-9
SMILES C1=CC=C(C=C1)NC(=O)CCCCCCC(=O)NO
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Corneal defectTransforming growth factor beta-1 proproteinP01137T9725726330748
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Gastrointestinal haemorrhage24.07.02.009; 07.12.02.001--Not Available
Guillain-Barre syndrome17.09.01.001; 11.07.01.001; 10.04.10.005--
Haematemesis24.07.02.011; 07.12.02.0020.000533%Not Available
Haemoptysis24.07.01.006; 22.02.03.004; 02.01.02.006--Not Available
Headache17.14.01.0010.001066%
Hydrocephalus17.07.01.0010.000533%
Hyperglycaemia14.06.02.002; 05.06.02.002--
Hypertension24.08.02.001--
Hypoaesthesia17.02.06.0230.000799%Not Available
Hypokalaemia14.05.03.0020.000533%
Hyponatraemia14.05.04.002--
Infection11.01.08.0020.000208%Not Available
Lethargy19.04.04.004; 17.02.04.003; 08.01.01.0080.000799%
Leukopenia01.02.02.001--Not Available
Loss of consciousness17.02.04.004--Not Available
Lymphocyte count decreased13.01.06.0060.000533%
Memory impairment19.20.01.003; 17.03.02.0030.000533%
Muscle spasms15.05.03.0040.000533%
Mycosis fungoides01.11.03.001; 23.07.04.008; 16.17.03.0010.000533%Not Available
Myelodysplastic syndrome16.01.04.001; 01.10.04.0010.000139%
Myocardial infarction24.04.04.009; 02.02.02.007--
Nausea07.01.07.0010.001865%
Neoplasm malignant16.16.01.001--Not Available
Neuropathy peripheral17.09.03.0030.000799%Not Available
Neutropenia01.02.03.004--Not Available
Neutrophil count decreased13.01.06.0100.000533%
Oedema peripheral14.05.06.011; 08.01.07.007; 02.05.04.007--
Pancytopenia01.03.03.003--Not Available
Pelvi-ureteric obstruction20.01.05.003--Not Available
Platelet count decreased13.01.04.0010.001332%
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