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

DYSPNOEA ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
PULMONARY ARTERY WALL HYPERTROPHY ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ACINETOBACTER INFECTION ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
CAROTID ARTERY DISSECTION ( 4 FDA reports)
CATHETER SEPSIS ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
ENTEROBACTER INFECTION ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
LIVEDO RETICULARIS ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PAIN ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
SERRATIA INFECTION ( 4 FDA reports)
VENOUS INSUFFICIENCY ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CARDIAC MURMUR FUNCTIONAL ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
SEASONAL ALLERGY ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ANGER ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
FALL ( 1 FDA reports)
GRANULOCYTES MATURATION ARREST ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM ( 1 FDA reports)
KETOSIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)

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