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

TRANSPLANT REJECTION ( 37 FDA reports)
BLOOD CREATININE INCREASED ( 34 FDA reports)
ILL-DEFINED DISORDER ( 31 FDA reports)
MEDICATION ERROR ( 25 FDA reports)
URINARY TRACT INFECTION ( 22 FDA reports)
TRANSPLANT FAILURE ( 20 FDA reports)
LEUKOPENIA ( 18 FDA reports)
VIRAL INFECTION ( 17 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 17 FDA reports)
NEPHROPATHY ( 17 FDA reports)
ENTEROCOCCAL INFECTION ( 17 FDA reports)
MENINGITIS ENTEROCOCCAL ( 17 FDA reports)
HAEMORRHAGIC ANAEMIA ( 17 FDA reports)
RENAL TUBULAR DISORDER ( 16 FDA reports)
PANCYTOPENIA ( 16 FDA reports)
NEPHROSCLEROSIS ( 15 FDA reports)
DRUG DISPENSING ERROR ( 14 FDA reports)
PYREXIA ( 7 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 6 FDA reports)
INFECTION ( 6 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
DRUG PRESCRIBING ERROR ( 5 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
RENAL FAILURE ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
EPIGLOTTIC OEDEMA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATITIS ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CHILLS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
TREMOR ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)

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