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

NEUTROPENIA ( 12 FDA reports)
SEPTIC SHOCK ( 12 FDA reports)
SEPSIS ( 12 FDA reports)
INTESTINAL OBSTRUCTION ( 12 FDA reports)
ALLODYNIA ( 6 FDA reports)
RESPIRATORY DEPRESSION ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
VOMITING ( 4 FDA reports)
PULMONARY INFARCTION ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
NARCOTIC INTOXICATION ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
PAIN ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
EMPHYSEMA ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
MALIGNANT ASCITES ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
BONE MARROW TRANSPLANT ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
PNEUMONIA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ANURIA ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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