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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126857951 | 12685795 | 1 | I | 20160121 | 20160125 | 20160825 | 20160825 | PER | US-NOVOPROD-478866 | NOVO NORDISK | 45.00 | YR | A | M | Y | 0.00000 | 20160825 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126857951 | 12685795 | 1 | PS | VICTOZA | LIRAGLUTIDE | 1 | Subcutaneous | 0.6 MG, QD | N | ES6V754 | 22341 | .6 | MG | SOLUTION FOR INJECTION | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126857951 | 12685795 | 1 | Type 2 diabetes mellitus |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126857951 | 12685795 | Abdominal discomfort | |
| 126857951 | 12685795 | Chills | |
| 126857951 | 12685795 | Diarrhoea | |
| 126857951 | 12685795 | Headache | |
| 126857951 | 12685795 | Muscle spasms | |
| 126857951 | 12685795 | Night sweats |
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 |
|---|---|---|---|---|---|---|
| 126857951 | 12685795 | 1 | 20160121 | 20160123 | 0 |