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

URINARY RETENTION ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
BLADDER PAIN ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
DISORIENTATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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