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

RHABDOMYOLYSIS ( 7 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
FALL ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
URINE COLOUR ABNORMAL ( 5 FDA reports)
ABDOMINAL ABSCESS ( 4 FDA reports)
ABDOMINAL NEOPLASM ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DEATH ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
RASH ( 4 FDA reports)
ATAXIA ( 3 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
COLITIS MICROSCOPIC ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LIPID METABOLISM DISORDER ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POLYP ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TUMOUR HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPULSE-CONTROL DISORDER ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OCULOGYRATION ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL INTESTINE CARCINOMA ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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