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

SHOCK ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
COLON CANCER ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
SEPSIS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
ULCER ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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