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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6660707 | 7303706 | F | 6660707-2 | 20100222 | 20100322 | 20100331 | EXP | US-SANOFI-AVENTIS-2010SA011194 | SANOFI-AVENTIS | 64 | YR | F | Y | 20100331 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6660707 | 1013418269 | PS | OPTICLICK | 2 | E001 | 21629 | |||||
| 6660707 | 1013418270 | SS | LANTUS | 1 | SUBCUTANEOUS | DOSE:60 UNIT(S) | C254 | 021081 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6660707 | 1013418269 | DIABETES MELLITUS |
| 6660707 | 1013418270 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6660707 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6660707 | HYPERHIDROSIS |
| 6660707 | HYPOGLYCAEMIA |
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 |
|---|---|---|---|---|---|
| 6660707 | 1013418269 | 20060101 | |||
| 6660707 | 1013418270 | 20060101 |