Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125689442 | 12568944 | 2 | F | 20160713 | 20160719 | 20160721 | EXP | DK-DKMA-ADR 23556493 | DK-ACCORD-042319 | ACCORD | 73.00 | YR | F | Y | 0.00000 | 20160721 | MD | DK | DK |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125689442 | 12568944 | 1 | PS | ESCITALOPRAM | ESCITALOPRAM OXALATE | 1 | Y | 202389 | |||||||||||
125689442 | 12568944 | 2 | SS | BRINTELLIX | VORTIOXETINE HYDROBROMIDE | 1 | Y | 0 | 5 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125689442 | 12568944 | 1 | Major depression |
125689442 | 12568944 | 2 | Major depression |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125689442 | 12568944 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125689442 | 12568944 | Aggression | |
125689442 | 12568944 | Confusional state | |
125689442 | 12568944 | Drug ineffective | |
125689442 | 12568944 | Feeling abnormal | |
125689442 | 12568944 | Limb discomfort | |
125689442 | 12568944 | Muscle spasms |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125689442 | 12568944 | 1 | 20160329 | 20160418 | 0 | |
125689442 | 12568944 | 2 | 20160418 | 20160512 | 0 |