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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4869371 | 5924589 | F | 4869371-6 | 20051101 | 20051109 | 20051230 | EXP | US-AVENTIS-200519167US | AVENTIS PHARMACEUTICALS, INC. | F | Y | 20051230 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4869371 | 1006775823 | PS | LANTUS | 1 | DOSE: NOT PROVIDED | UNKNOWN | 21081 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4869371 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4869371 | LOSS OF CONSCIOUSNESS |
| 4869371 | PHARMACEUTICAL PRODUCT COMPLAINT |
| 4869371 | POOR QUALITY DRUG ADMINISTERED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |