Please choose an event type to view the corresponding MedsFacts report:

HYPERKALAEMIA ( 10 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
RENAL FAILURE ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
HYPOTENSION ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIALYSIS DISEQUILIBRIUM SYNDROME ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
ANURIA ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PALLOR ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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