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

INJECTION SITE PAIN ( 2 FDA reports)
ANGER ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELASH THICKENING ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)

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