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

FALL ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
NAUSEA ( 5 FDA reports)
FATIGUE ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ADRENAL MASS ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ADHESION ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HIP DEFORMITY ( 1 FDA reports)
HYPERPARATHYROIDISM PRIMARY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MASS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRESS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)

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