Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Anagrelide
Drug ID BADD_D00139
Description Anagrelide is a platelet-reducing agent used to lower dangerously elevated platelet levels (i.e. to treat thrombocythemia) in patients with myeloproliferative neoplasms.[L14153] It is an oral imidazoquinazoline that was first approved for use in the US in 1997.[A214274] It appears to carry a better response rate than other thrombocythemia treatments (e.g. [busulfan], [hydroxyurea]) and may be better tolerated.[A214274]
Indications and Usage Anagrelide is indicated for the treatment of thrombocythemia, secondary to malignant neoplasms, to reduce platelet count and the associated risk of thrombosis. It is also beneficial in the amelioration of thrombocythemia symptoms including thrombo-hemorrhagic events.[L14153]
Marketing Status approved
ATC Code L01XX35
DrugBank ID DB00261
KEGG ID D07455
MeSH ID C021139
PubChem ID 135409400
TTD Drug ID D0D1HW
NDC Product Code 13668-462; 13668-453
UNII K9X45X0051
Synonyms anagrelide | Agrylin | BL 4162A | Agrelin | anagrelide hydrochloride | imidazo(2,1-b)quinazolin-2(3H)-one, 6,7-dichloro-1,5-dihydro-, monohydrochloride | 6,7-dichloro-1,5-dihydroimidazo(2,1-b)quinazolin-2(3H)-one hydrochloride
Chemical Information
Molecular Formula C10H7Cl2N3O
CAS Registry Number 68475-42-3
SMILES C1C2=C(C=CC(=C2Cl)Cl)N=C3N1CC(=O)N3
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)
Cellulitis11.02.01.001; 23.11.02.004--Not Available
Cerebral haemorrhage24.07.04.001; 17.08.01.0030.000112%Not Available
Cerebral infarction24.04.06.002; 17.08.01.0040.000336%Not Available
Cerebrovascular accident24.03.05.001; 17.08.01.007--
Chest pain02.02.02.011; 22.12.02.003; 08.01.08.0020.000112%Not Available
Chills15.05.03.016; 08.01.09.001--
Chronic myeloid leukaemia16.01.07.001; 01.10.07.001--Not Available
Colitis07.08.01.001--
Condition aggravated08.01.03.0040.000224%Not Available
Confusional state19.13.01.001; 17.02.03.005--
Conjunctivitis11.01.06.012; 06.04.01.002--
Constipation07.02.02.001--
Coordination abnormal17.02.02.004--Not Available
Cough22.02.03.0010.000224%
Dehydration14.05.05.001--
Depression19.15.01.001--
Dermatitis23.03.04.002--Not Available
Diarrhoea07.02.01.001--
Diplopia17.17.01.005; 06.02.06.002--Not Available
Discomfort08.01.08.0030.000168%Not Available
Dizziness02.11.04.006; 24.06.02.007; 17.02.05.003--
Dry mouth07.06.01.002--
Dry skin23.03.03.001--
Duodenal ulcer07.04.02.002--
Dysarthria17.02.08.001; 19.19.03.001--
Dyspepsia07.01.02.001--
Dysphagia07.01.06.0030.000358%
Dyspnoea22.02.01.004; 02.11.05.0030.000560%
Dyspnoea paroxysmal nocturnal02.11.05.006; 22.02.01.0180.000112%Not Available
Dysuria20.02.02.002--
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ADReCS-Target
Drug Name ADR Term Target
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