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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125462581 | 12546258 | 1 | I | 20160531 | 20160628 | 20160711 | 20160711 | EXP | PK-NOVOPROD-499202 | NOVO NORDISK | 50.00 | YR | A | M | Y | 0.00000 | 20160711 | OT | PK | PK |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125462581 | 12546258 | 1 | PS | VICTOZA | LIRAGLUTIDE | 1 | Unknown | 0.6 MG, QD | FS6X723 | 22341 | .6 | MG | SOLUTION FOR INJECTION | QD | |||||
125462581 | 12546258 | 2 | SS | VICTOZA | LIRAGLUTIDE | 1 | 22341 | SOLUTION FOR INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125462581 | 12546258 | 1 | Glucose tolerance impaired |
125462581 | 12546258 | 2 | Obesity |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125462581 | 12546258 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125462581 | 12546258 | Abdominal discomfort | |
125462581 | 12546258 | Dyspepsia | |
125462581 | 12546258 | Nausea | |
125462581 | 12546258 | Off label use | |
125462581 | 12546258 | Vomiting |
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 |
---|---|---|---|---|---|---|
125462581 | 12546258 | 1 | 20160531 | 201606 | 0 |