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a non-interventional post-authorisation safety study was conducted which involved 300 patients undergoing vascular surgery during which evicel was used.
300 patsiendil, kes läbisid veresoonte operatsiooni, mille käigus kasutati eviceli, viidi läbi müügiloa saamise järgne mittesekkuv ohutusuuring.
additionally, 1 non-serious case of ‘light adaptation difficulties’ (not resolved) was reported in the non-interventional study inject.
lisaks teatati mittesekkuvas uuringus inject ühest mittetõsisest “valgusega kohandumise raskuste” juhust (ei lahenenud).
a non-interventional study to evaluate the occurrence of neurological and ophthalmic adverse events (to be coded using the relevant veddra terminology) in dogs treated with trifexis.
ravisse mittesekkuv uuring, et hinnata neuroloogiliste ja oftalmoloogiliste kõrvaltoimete tekkimist (kodeeritult, kasutades asjakohast veddra terminoloogiat) koertel, keda ravitakse trifexisega.
data have been obtained from clinical studies in 61 children under 6 years of age and non-interventional studies in children of all ages.
andmed on olemas kuni 6- aastaste 61 lapse kohta kliinilistest uuringutest ja igas vanuses laste kohta mitteinterventsionaalsetest uuringutest.
non-interventional post-authorisation safety study (pass): study 20150136: an observational study of blinatumomab safety and effectiveness, utilisation, and treatment practices*
müügiloa saamise järgne mittesekkuv ohutusuuring: uuring 20150136 – blinatumomabi ohutuse, kasutamise ja ravipraktika jälgimisuuring