any information collected related to AE that cannot be mapped to standard variables will be stored in suppae... there is one standard qnam AETRTEM which is used in most studies..
sure, will try to do it.. EC and EX belong to interventions class - some of the variables can be remembered using CM concpet map. Link to CM video is below. ua-cam.com/video/SKTV9e65NTA/v-deo.html
Hi, the information on whether an adverse event is a dose limiting toxicity is generally captured on crf page itself. There is no standard variable in SDTM IG to indicate dose limiting toxicities. So, the information will be mapped to SUPPAE.
Hi Sir, I need a information on event and findings domain. Sorting data set on basis of USUBJID AETESTCD AESTDTC is correct or USUBJID AETESTCD AESTDTC is correct ?
There is no standard sorting requirement, you can choose it based on your requirement. I am assuming you have inadvertently specified AE as a findings domain here. AE is an events domain and you dont have 'AETESTCD'.
i felt so easy to remember AE domain, really super explanation.
Glad it helped!
Very nice session.Could you please explain the difference between AESOC and AEBODSYS
Sure, coming soon..
beautiful session on AE domain
Glad you liked it Shweta!
Hi Dude Your videos are very helpful , Can you please do video on which type of data will be collect in SUPPAE Domain...?
any information collected related to AE that cannot be mapped to standard variables will be stored in suppae... there is one standard qnam AETRTEM which is used in most studies..
Thank you sir it is very helpful information to us .can we expect more information from you
Yes, sure
thanks. Can you please arrange them in order like SDTM separate and ADaM separate from beginning till end.
sure Arjun, will clean up the playlists over next few days
Excellent
Thank you..
Sir please make video on ex and ec domain variables.
sure, will try to do it.. EC and EX belong to interventions class - some of the variables can be remembered using CM concpet map. Link to CM video is below.
ua-cam.com/video/SKTV9e65NTA/v-deo.html
hi sir how do you map the dose limiting toxicities in the sdtm ae domain
Hi, the information on whether an adverse event is a dose limiting toxicity is generally captured on crf page itself. There is no standard variable in SDTM IG to indicate dose limiting toxicities. So, the information will be mapped to SUPPAE.
How will we populate serious criterion variables (AESCONG AESLIFE AESCAN etc.) if aeser="Y"?
Hi Venkat, we do not derive them. Information for these variables has to be collected on the CRF.
@@mycsg okay
@@mycsg will have a data about those variables in raw datasets?
@@venkateswararaovummadi1935 , yes.
Hi Sir, I need a information on event and findings domain.
Sorting data set on basis of USUBJID AETESTCD AESTDTC is correct or USUBJID AETESTCD AESTDTC is correct ?
There is no standard sorting requirement, you can choose it based on your requirement. I am assuming you have inadvertently specified AE as a findings domain here. AE is an events domain and you dont have 'AETESTCD'.