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

THROMBOCYTOPENIA ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
RESPIRATORY DEPRESSION ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PAIN ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
PNEUMONIA ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
ROTAVIRUS TEST POSITIVE ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
FALL ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
AGITATION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
TRANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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