Adverse Drug Reaction Classification System

         

ADR Ontology
ADR Term Drug level increased
ADR ID BADD_A01338
ADR Hierarchy
13      Investigations
13.17      Toxicology and therapeutic drug monitoring
13.17.01      Therapeutic drug monitoring analyses
13.17.01.004      Drug level increased
Description Not Available
MedDRA Code 10013722
MeSH ID Not Available
ADR Severity Grade (FAERS) Not Available
ADR Severity Grade (CTCAE) Not Available
Synonym
Drug level in blood increased | Drug level increased | Drug level NOS CSF increased | Drug level NOS increased | Raised drug level | Raised drug levels in blood | Raised drug levels in cerebrospinal fluid
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D00214Basiliximab--
BADD_D00374Carvedilol--
BADD_D00475Citalopram--
BADD_D00696Divalproex sodium--
BADD_D00809Escitalopram--
BADD_D01003Ganciclovir--
BADD_D01265Levetiracetam--
BADD_D01455Micafungin--
BADD_D01502Moxifloxacin hydrochloride--
BADD_D01507Mycophenolate mofetil--
BADD_D01835Pregabalin--
BADD_D01966Ropinirole--
BADD_D02105Tacrolimus--
BADD_D02329Valproic acid--
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ADReCS-Target
ADR Term Drug Name Target