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

HYPOGLYCAEMIA ( 6 FDA reports)
DIZZINESS ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
FALL ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
COMA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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