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

INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
ULCER ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use