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)
Abdominal discomfort07.01.06.001--Not Available
Abdominal pain07.01.05.002--
Acute myocardial infarction24.04.04.001; 02.02.02.0010.000392%Not Available
Alopecia23.02.02.001--
Amblyopia06.02.01.001--Not Available
Amnesia17.03.02.001; 19.20.01.001--
Anaemia01.03.02.0010.000112%
Angina pectoris24.04.04.002; 02.02.02.0020.000112%
Aphthous ulcer07.05.06.002--Not Available
Arrhythmia02.03.02.0010.000168%Not Available
Arrhythmia supraventricular02.03.03.001--Not Available
Arthralgia15.01.02.001--
Arthritis15.01.01.001--
Asthenia08.01.01.001--Not Available
Asthma22.03.01.002; 10.01.03.010--Not Available
Atrial fibrillation02.03.03.002--
Atrioventricular block complete02.03.01.003--
Back pain15.03.04.005--
Blood creatinine increased13.13.01.004--
Body temperature increased13.15.01.001--Not Available
Bone pain15.02.01.001--
Breast cancer21.05.01.003; 16.10.01.0010.000112%Not Available
Bronchitis11.01.09.001; 22.07.01.001--
Cardiac arrest02.03.04.0010.000280%
Cardiac failure02.05.01.0010.000112%
Cardiac failure congestive02.05.01.002--Not Available
Cardio-respiratory arrest22.02.06.007; 02.03.04.0020.000112%Not Available
Cardiomegaly02.04.02.001--Not Available
Cardiomyopathy02.04.01.0010.000112%Not Available
Cardiovascular disorder02.11.01.010; 24.03.02.009--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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