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

INTERSTITIAL LUNG DISEASE ( 14 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 11 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
HYPOKALAEMIA ( 10 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
ASCITES ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TORSADE DE POINTES ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
MELAENA ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
RASH ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACETONAEMIC VOMITING ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CHEILITIS ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GLOSSITIS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 3 FDA reports)
LIPIDS INCREASED ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
THIRST ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TINEA VERSICOLOUR ( 3 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VENTRICULAR FLUTTER ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADRENAL ATROPHY ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOKING ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
METAMYELOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MYELOCYTE PRESENT ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE NECROSIS ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENIN DECREASED ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THYMECTOMY ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)

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