Adverse Drug Reaction Classification System

ADR Ontology
ADR Term Red blood cell count increased
ADR ID BADD_A03720
ADR Hierarchy
13      Investigations
13.01      Haematology investigations (incl blood groups)
13.01.05      Red blood cell analyses
13.01.05.008      Red blood cell count increased
Description Not Available
MedDRA Code 10038155
MeSH ID Not Available
ADR Severity Grade (FAERS)
ADR Severity Grade (CTCAE) Not Available
Synonym
RBC count increased | Red blood cell count high | Red blood cell count increased | Erythrocytes increased
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_D00036Acitretin--
BADD_D00190Atropine sulfate--
BADD_D00193Axitinib0.000533%
BADD_D00344Canagliflozin0.000766%
BADD_D00511Clozapine0.053246%
BADD_D00574Dalfampridine0.002614%
BADD_D00576Danazol--
BADD_D00856Etoricoxib--
BADD_D01013Gemifloxacin--
BADD_D01014Gemifloxacin mesylate--
BADD_D01119Ibrutinib0.000533%
BADD_D01253Lenalidomide0.005790%
BADD_D01336Macitentan0.000577%
BADD_D01567Nilotinib0.000533%
BADD_D01835Pregabalin0.000236%
BADD_D01978Ruxolitinib0.001066%
BADD_D02047Sodium oxybate0.001211%
BADD_D02170Testosterone0.001188%
BADD_D02174Testosterone undecanoate--
BADD_D02254Tramadol--
BADD_D02464Fingolimod0.004053%
BADD_D02510Rucaparib0.001066%
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