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PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 6 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 5 FDA reports)
HYPERTENSIVE CRISIS ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
DEATH ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
FEMORAL ARTERY OCCLUSION ( 4 FDA reports)
GANGRENE ( 4 FDA reports)
INTERMITTENT CLAUDICATION ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
PERIPHERAL ISCHAEMIA ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MUSCLE SPASTICITY ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PAIN ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
ULCER ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VASCULAR GRAFT ( 3 FDA reports)
VASCULAR OPERATION ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BONE TRIMMING ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SEQUESTRECTOMY ( 2 FDA reports)
THROMBECTOMY ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
FALL ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENSION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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