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DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
RESPIRATORY PARALYSIS ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
STRESS CARDIOMYOPATHY ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
THIRST ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)

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