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

INFUSION RELATED REACTION ( 7 FDA reports)
SHOCK ( 6 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
EXPOSURE VIA FATHER ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
SUDDEN VISUAL LOSS ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
COLITIS ISCHAEMIC ( 2 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
DYSGEUSIA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
APHASIA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)

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