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

DRUG INTERACTION ( 9 FDA reports)
FALL ( 9 FDA reports)
SOMNOLENCE ( 8 FDA reports)
HYPOTENSION ( 6 FDA reports)
BLOOD IRON DECREASED ( 5 FDA reports)
AGITATION ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
COMA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
GASTRIC POLYPS ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
JOINT DISLOCATION ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
TREMOR ( 3 FDA reports)
UPPER LIMB FRACTURE ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD FOLATE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BULIMIA NERVOSA ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS GRANULOMATOUS ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MICROLITHIASIS ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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