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

VOMITING ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MALAISE ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
DEATH ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
MILK-ALKALI SYNDROME ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)

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