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

RENAL FAILURE ACUTE ( 9 FDA reports)
ASCITES ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
VERTIGO ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
RASH ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
POLYMYOSITIS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
MALAISE ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
ANURIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
DYSURIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
AGITATION ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
APLASIA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
PLASMACYTOSIS ( 2 FDA reports)
COMA ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DEATH ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)

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