Adverse Drug Reaction Classification System

         

ADR Ontology
ADR Term Blood potassium increased
ADR ID BADD_A00589
ADR Hierarchy
13      Investigations
13.11      Water, electrolyte and mineral investigations
13.11.01      Mineral and electrolyte analyses
13.11.01.011      Blood potassium increased
Description Not Available
MedDRA Code 10005725
MeSH ID Not Available
ADR Severity Grade (FAERS) Not Available
ADR Severity Grade (CTCAE) Not Available
Synonym
Blood potassium increased | Elevated K | K+ increased | Plasma potassium increased | Potassium high | Potassium increased | Potassium retention | Potassium serum increased | Serum potasium increased | Serum potassium increased
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D01375Meloxicam sodium--
BADD_D01530Nandrolone decanoate--
BADD_D01587Norfloxacin--
BADD_D01602Olmesartan--
BADD_D01634Oxandrolone--
BADD_D01668Pantoprazole--
BADD_D01687Pazopanib--
BADD_D01688Pazopanib hydrochloride--
BADD_D01799Ponatinib--
BADD_D01800Ponatinib hydrochloride--
BADD_D01834Prednisone--
BADD_D01909Ramipril--
BADD_D02031Sitaxentan--
BADD_D02100Sunitinib--
BADD_D02101Sunitinib malate--
BADD_D02254Tramadol--
BADD_D02259Trandolapril--
BADD_D02331Valsartan--
BADD_D02334Vandetanib--
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