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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125861331 | 12586133 | 1 | I | 20160622 | 20160622 | 20160725 | 20160725 | PER | US-ASTRAZENECA-2016SE69412 | ASTRAZENECA | 0.00 | Y | 0.00000 | 20160725 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125861331 | 12586133 | 1 | PS | BYDUREON | EXENATIDE | 1 | Unknown | UNKNOWN | 22200 | ||||||||||
| 125861331 | 12586133 | 2 | SS | BYETTA | EXENATIDE | 1 | Unknown | UNKNOWN | 0 | SOLUTION FOR INJECTION IN PRE-FILLED PEN |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125861331 | 12586133 | Blood glucose increased | |
| 125861331 | 12586133 | Decreased appetite | |
| 125861331 | 12586133 | Hunger |
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 |
|---|---|---|---|---|---|---|
| 125861331 | 12586133 | 1 | 20160621 | 0 |