Adverse Drug Reaction Classification System

ADR Ontology
ADR Term Device malfunction
ADR ID BADD_A06205
ADR Hierarchy
27      Product issues
27.01      Device issues
27.01.02      Device malfunction events NEC
27.01.02.002      Device malfunction
Description Not Available
MedDRA Code 10063829
MeSH ID Not Available
ADR Severity Grade (FAERS) Not Available
ADR Severity Grade (CTCAE) Not Available
Synonym
Cardiac pacemaker malfunction | Ventriculoperitoneal shunt malfunction | Implantable defibrillator malfunction | Inappropriate pacemaker firing | Device malfunction | Peritoneal catheter dysfunction | Prosthesis closing defect | Prosthesis opening defect | Mechanical device firing issue | Incomplete device expansion | Automated external defibrillator malfunction | Device motor malfunction | Device component malfunction | Device delivery system malfunction | Pump motor stall | Catheter dysfunction | Diagnostic device malfunction | Dose counter malfunction | Premature device expansion | Device inappropriate reset | Device reset issue | Device failure to cycle | Device failure to align | Device misfire | Device failure to self-test | Device suction event | Ventricular assist device suction event | Removable device component cannot be removed | Auto-injector viewing window blocked
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D00086Alprostadil--
BADD_D00808Erythropoietin--
BADD_D01101Hydroxybutanedial--
BADD_D02018Sildenafil--
BADD_D02217Tigecycline--
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