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

BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE PROTEIN, QUANTITATIVE ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)

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