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

BLOOD GLUCOSE INCREASED ( 5 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
VOMITING ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
CHILLS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)

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