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BLOOD GLUCOSE INCREASED ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
VOMITING ( 4 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
FALL ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
PAIN ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CATARACT OPERATION ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHILLS ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
GLUCOSE URINE PRESENT ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CD4/CD8 RATIO INCREASED ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYST ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIAPHRAGMATIC INJURY ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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