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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127380751 | 12738075 | 1 | I | 2016 | 20160822 | 20160912 | 20160912 | PER | US-SA-2016SA154714 | AVENTIS | 72.00 | YR | E | M | Y | 0.00000 | 20160912 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127380751 | 12738075 | 1 | PS | SOLOSTAR | DEVICE | 1 | 6F231A | 206538 | QD | ||||||||||
| 127380751 | 12738075 | 2 | SS | TOUJEO | INSULIN GLARGINE | 1 | Unknown | 6F231A | 206538 | INJECTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127380751 | 12738075 | 1 | Type 2 diabetes mellitus |
| 127380751 | 12738075 | 2 | Type 2 diabetes mellitus |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127380751 | 12738075 | Blood glucose abnormal | |
| 127380751 | 12738075 | Device issue | |
| 127380751 | 12738075 | Wrong technique in product usage process |
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 |
|---|---|---|---|---|---|---|
| 127380751 | 12738075 | 1 | 201605 | 0 | ||
| 127380751 | 12738075 | 2 | 201605 | 0 |