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

TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DEATH ( 3 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
ANGIOTENSIN I DECREASED ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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