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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6768336 | 7357555 | F | 6768336-7 | 20080501 | 20100608 | 20100614 | PER | US-SANOFI-AVENTIS-2010SA020664 | SANOFI-AVENTIS | 54 | YR | F | Y | 86.2 | KG | 20100614 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6768336 | 1013860743 | PS | LANTUS | 1 | SUBCUTANEOUS | DOSE:88 UNIT(S) | UNKNOWN | 21081 | |||
| 6768336 | 1013860744 | SS | LANTUS | 1 | SUBCUTANEOUS | 34 UNITS IN AM AND 58 IN PM | 021081 | ||||
| 6768336 | 1013860745 | SS | SOLOSTAR | 2 | UNKNOWN | 021081 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6768336 | 1013860743 | TYPE 2 DIABETES MELLITUS |
| 6768336 | 1013860745 | TYPE 2 DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6768336 | HO |
| 6768336 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6768336 | BLINDNESS |
| 6768336 | CORONARY ARTERY BYPASS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6768336 | 1013860743 | 20070101 | |||
| 6768336 | 1013860745 | 20070101 |