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

RESPIRATORY FAILURE ( 9 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
UNRESPONSIVE TO STIMULI ( 7 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HYDROCELE ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
NOCARDIOSIS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
STENOTROPHOMONAS INFECTION ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ANAPHYLACTOID SHOCK ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PHAEOCHROMOCYTOMA ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RETINAL INFARCTION ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BASILAR ARTERY THROMBOSIS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FAMILIAL HAEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYELONEPHRITIS FUNGAL ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCAB ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROID HAEMORRHAGE ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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