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

ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
HEART RATE DECREASED ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
ASCITES ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CUSHING'S SYNDROME ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
HYPOALDOSTERONISM ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
LIDDLE'S SYNDROME ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GLOSSOPTOSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENIN DECREASED ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
FALL ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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