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

INTESTINAL OBSTRUCTION ( 12 FDA reports)
PANCREATITIS ( 12 FDA reports)
ANAEMIA ( 7 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
FALL ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
ADRENAL INSUFFICIENCY ( 4 FDA reports)
ADRENAL NEOPLASM ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
MALAISE ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GENITAL ULCERATION ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADRENAL GLAND CANCER METASTATIC ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILIARY TRACT OPERATION ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
NECROSIS OF ARTERY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATIC DUCT DILATATION ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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