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

RENAL FAILURE ( 11 FDA reports)
PYREXIA ( 10 FDA reports)
PNEUMONIA ( 8 FDA reports)
CORONARY ARTERY DISEASE ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
COLITIS ULCERATIVE ( 6 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
MENINGITIS ( 5 FDA reports)
PANCREATITIS ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CAROTID ARTERY STENOSIS ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
COUGH ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
GASTRIC ULCER PERFORATION ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
MITRAL VALVE DISEASE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
CORONARY ANGIOPLASTY ( 3 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
LEFT ATRIAL DILATATION ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
AGEUSIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CORONARY ARTERY ANEURYSM ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
DEATH ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ADAMS-STOKES SYNDROME ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMAUROSIS FUGAX ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST NEGATIVE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTPERICARDIOTOMY SYNDROME ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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