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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126257921 | 12625792 | 1 | I | 20160226 | 20160726 | 20160805 | 20160805 | EXP | FR-NOVOPROD-503663 | NOVO NORDISK | 73.00 | YR | E | M | Y | 71.00000 | KG | 20160805 | MD | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126257921 | 12625792 | 1 | PS | VICTOZA | LIRAGLUTIDE | 1 | Subcutaneous | 1.2 MG, QD | 4.7849998 | MG | Y | UNKNOWN | 22341 | 1.2 | MG | SOLUTION FOR INJECTION | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126257921 | 12625792 | 1 | Type 2 diabetes mellitus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126257921 | 12625792 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126257921 | 12625792 | Abdominal pain upper | |
| 126257921 | 12625792 | Decreased appetite | |
| 126257921 | 12625792 | Gastritis | |
| 126257921 | 12625792 | Gastrooesophageal reflux disease | |
| 126257921 | 12625792 | Hepatitis | |
| 126257921 | 12625792 | Pancreatitis | |
| 126257921 | 12625792 | 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 |
|---|---|---|---|---|---|---|
| 126257921 | 12625792 | 1 | 20160222 | 20160608 | 0 |