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

DRUG INTERACTION ( 12 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
TORSADE DE POINTES ( 10 FDA reports)
MYOCLONIC EPILEPSY ( 8 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
ACCIDENTAL OVERDOSE ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
RENAL TUBULAR ACIDOSIS ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
PAIN ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
COLITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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