Adverse Drug Reaction Classification System

ADR Ontology
ADR Term Full blood count decreased
ADR ID BADD_A07233
ADR Hierarchy
13      Investigations
13.01      Haematology investigations (incl blood groups)
13.01.07      Blood counts NEC
13.01.07.004      Full blood count decreased
Description Not Available
MedDRA Code 10017413
MeSH ID Not Available
ADR Severity Grade (FAERS)
ADR Severity Grade (CTCAE) Not Available
Synonym
Full blood count decreased | Full blood count reduced
ADR Related Proteins
Protein Name UniProt AC TTD Target ID
Not AvailableNot AvailableNot Available
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D00014Abiraterone--
BADD_D00151Apixaban--
BADD_D00156Apremilast--
BADD_D00194Azacitidine0.006127%
BADD_D00284Bortezomib0.001865%
BADD_D00285Bosentan--
BADD_D00286Bosutinib--
BADD_D00349Capecitabine--
BADD_D00356Carbamazepine--
BADD_D00364Carboplatin--
BADD_D00367Carfilzomib0.003197%
BADD_D00474Cisplatin--
BADD_D00511Clozapine--
BADD_D00535Crizotinib--
BADD_D00589Dasatinib0.007460%
BADD_D00594Deferasirox--
BADD_D00623Dexamethasone0.003090%
BADD_D00680Dimethyl fumarate--
BADD_D00732Droxidopa--
BADD_D00734Duloxetine--
BADD_D00759Eltrombopag0.003812%
BADD_D00775Enzalutamide--
BADD_D00858Everolimus--
BADD_D01009Gemcitabine--
BADD_D01136Imatinib--
BADD_D01223Ixazomib0.002931%
BADD_D01253Lenalidomide1.154509%
BADD_D01257Letrozole--
BADD_D01295Linezolid--
BADD_D01313Lomustine0.000533%
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