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

HYPERTENSION ( 20 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 20 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 19 FDA reports)
INFLAMMATION ( 19 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 19 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 14 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
ABSCESS LIMB ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
CARDIAC FAILURE ( 11 FDA reports)
ARTHRITIS BACTERIAL ( 10 FDA reports)
ASTHENIA ( 10 FDA reports)
OEDEMA PERIPHERAL ( 9 FDA reports)
DIARRHOEA ( 8 FDA reports)
HEPATIC FAILURE ( 8 FDA reports)
DIZZINESS ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
HYPOCALCAEMIA ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
SHOCK ( 6 FDA reports)
VOMITING ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
CARDIAC TAMPONADE ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
HYPOMAGNESAEMIA ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CHOLESTATIC LIVER INJURY ( 3 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HEPATIC CIRRHOSIS ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
CIRCUMORAL OEDEMA ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)

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