Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7300033 | 7817748 | I | 7300033-1 | 20110127 | 20110217 | EXP | US-SANOFI-AVENTIS-2011SA009016 | SANOFI-AVENTIS | YR | Y | 20110217 | PH | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7300033 | 1015809920 | PS | LANTUS | 1 | SUBCUTANEOUS | 0F503A | 021081 | ||||
| 7300033 | 1015809919 | SS | SOLOSTAR | 2 | SUBCUTANEOUS | 0F503A |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7300033 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7300033 | DEVICE MALFUNCTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |