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

VOMITING ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
CORONARY ARTERY THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
FOETOR HEPATICUS ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
CORONARY ARTERY REOCCLUSION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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