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

CONDITION AGGRAVATED ( 24 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
HYPOPROTEINAEMIA ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
AMMONIA INCREASED ( 5 FDA reports)
BURSITIS ( 5 FDA reports)
DECREASED ACTIVITY ( 5 FDA reports)
FALL ( 5 FDA reports)
FEMORAL NECK FRACTURE ( 5 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
PAPILLOPHLEBITIS ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
QUALITY OF LIFE DECREASED ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RADIUS FRACTURE ( 4 FDA reports)
VASCULAR CALCIFICATION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FRACTURE DELAYED UNION ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
ULNA FRACTURE ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENDOCARDITIS CANDIDA ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BLOOD AMINO ACID LEVEL INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAND FRACTURE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE TRANSFORMATION TEST POSITIVE ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MITRAL VALVE STENOSIS ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMALACIA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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