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

HYPERGLYCAEMIA ( 4 FDA reports)
CONSTIPATION ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
ASTHENIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
TREMOR ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
RASH ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
INDURATION ( 1 FDA reports)

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