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

OFF LABEL USE ( 20 FDA reports)
EYE OPERATION COMPLICATION ( 16 FDA reports)
PRODUCT QUALITY ISSUE ( 15 FDA reports)
GRAFT COMPLICATION ( 7 FDA reports)
HYPOTENSION ( 6 FDA reports)
POST PROCEDURAL HAEMATOMA ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
PNEUMONIA ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
PERINEAL ABSCESS ( 2 FDA reports)
PAIN ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
ARTERIOVENOUS FISTULA ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
FISTULA ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
SCLERAL GRAFT ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
AIR EMBOLISM ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
FEAR ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
END-TIDAL CO2 DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
DEATH ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONJUNCTIVAL OPERATION ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
AGITATION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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