Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Amifostine
Drug ID BADD_D00102
Description A phosphorothioate proposed as a radiation-protective agent. It causes splenic vasodilation and may block autonomic ganglia.
Indications and Usage For reduction in the cumulative renal toxicity in patients with ovarian cancer (using cisplatin) and moderate to severe xerostomia in patients undergoing post-operative radiation treatment for head and neck cancer.
Marketing Status approved; investigational
ATC Code V03AF05
DrugBank ID DB01143
KEGG ID D00226
MeSH ID D004999
PubChem ID 2141
TTD Drug ID D06CIE
NDC Product Code 76310-017; 46439-8768; 22568-8865; 60269-275; 61662-0003
UNII M487QF2F4V
Synonyms Amifostine | APAETP | Aminopropylaminoethylthiophosphoric Acid | S-(N-(3-Aminopropyl)-2-aminoethyl)thiophosphoric Acid | Gammaphos | Ethiofos | Amifostine Disodium Salt | Amifostine Monohydrate | Amifostine Trihydrate | Aminopropylaminoethylthiophosphate | Aminopropyl Aminoethylthiophosphate | Ethyol | NSC-296961 | NSC 296961 | NSC296961 | Amifostine Anhydrous | Ethiofos Anhydrous | WR-2721 | WR 2721 | WR2721 | YM-08310 | YM 08310 | YM08310 | Ethanethiol, 2-((3-aminopropyl)amino)-, dihydrogen phosphate (ester), trihydrate | Amifostine Monohydrochloride
Chemical Information
Molecular Formula C5H15N2O3PS
CAS Registry Number 20537-88-6
SMILES C(CN)CNCCSP(=O)(O)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)
Hypoxia22.02.02.003--
Laryngeal oedema23.04.01.005; 22.04.02.001; 10.01.05.003--
Loss of consciousness17.02.04.004--Not Available
Malaise08.01.01.003--
Myocardial infarction02.02.02.007; 24.04.04.009--
Myocardial ischaemia24.04.04.010; 02.02.02.008--Not Available
Nausea07.01.07.001--
Pruritus23.03.12.001--
Pyrexia08.05.02.003--
Rash23.03.13.001--Not Available
Renal failure20.01.03.005--Not Available
Respiratory arrest22.02.01.009--Not Available
Respiratory disorder22.02.07.002--Not Available
Seizure17.12.03.001--
Shock24.06.02.002--Not Available
Sneezing22.12.03.024--
Somnolence19.02.05.003; 17.02.04.006--
Stevens-Johnson syndrome10.01.01.045; 23.03.01.007; 12.03.01.014; 11.07.01.005--
Supraventricular tachycardia02.03.03.012--
Syncope02.11.04.015; 24.06.02.012; 17.02.04.008--
Tachycardia02.03.02.007--Not Available
Toxic epidermal necrolysis23.03.01.008; 12.03.01.015; 11.07.01.006; 10.01.01.006--
Urticaria23.04.02.001; 10.01.06.001--
Vomiting07.01.07.003--
Muscle tightness15.05.03.007--Not Available
Acute coronary syndrome02.02.02.015; 24.04.04.011--Not Available
Cardiac flutter02.03.02.012--Not Available
Toxic skin eruption12.03.01.073; 23.03.05.003; 10.01.01.008--Not Available
Ill-defined disorder08.01.03.049--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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