Genmab — September 2016
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A serious adverse event (SAE) in human drug trials is defined as any untoward medical occurrence that at any dose
results in death,
is life-threatening
requires inpatient hospitalization or causes prolongation of existing hospitalization
results in persistent or significant disability/incapacity,
is a congenital anomaly/birth defect, or
requires intervention to prevent permanent impairment or damage.[1] -
Det kan være interaktion med andre lægemidler som kan være årsagen. Den slags er også vigtigt at få styr på.
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http://medwatch.dk/secure/Medicinal___Biotek/article9010301.ece Så har J&J brugt penge!
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Ang: SAE. Er det ikke netop formålet med studiet (altså at nå frem til, hvad der kan udløse en SAE)?
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Glæder mig allerede til beskos's indslag på Børsen play
det bliver nok underholdende som altid.....
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