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

UTERINE PROLAPSE ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FALL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
INJURY ( 1 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
POST CONCUSSION SYNDROME ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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