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

OVERDOSE ( 4 FDA reports)
FEMUR FRACTURE ( 4 FDA reports)
FALL ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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