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

MEMORY IMPAIRMENT ( 6 FDA reports)
DYSGRAPHIA ( 6 FDA reports)
COGNITIVE DISORDER ( 6 FDA reports)
MUSCLE RIGIDITY ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
CEREBELLAR INFARCTION ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PARAESTHESIA ORAL ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
FALL ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
BLISTER ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use