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

NAUSEA ( 2 FDA reports)
DEATH ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)

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