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

PRURITUS ( 6 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
MALIGNANT MELANOMA ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ANAL DISCOMFORT ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PSEUDOCYST ( 2 FDA reports)
RECTAL DISCHARGE ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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