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

BLOOD GLUCOSE INCREASED ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
HEADACHE ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MALAISE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
SWEAT GLAND DISORDER ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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