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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6082367 | 6912592 | I | 6082367-4 | 20081202 | 20090212 | 20090218 | EXP | FR-AVENTIS-200910710EU | SANOFI-AVENTIS | 86 | YR | F | Y | 20090218 | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6082367 | 1011144610 | PS | FLUDEX /00340101/ | 2 | ORAL | DOSE: UNK | 18538 | ||||
| 6082367 | 1011144611 | SS | LERCAN | 2 | ORAL | DOSE: UNK | |||||
| 6082367 | 1011144612 | C | TANAKAN /01003103/ | 2 | |||||||
| 6082367 | 1011144613 | C | TRIMEBUTINE | 2 | |||||||
| 6082367 | 1011144614 | C | FENOFIBRATE | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6082367 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6082367 | FALL |
| 6082367 | FEMUR FRACTURE |
| 6082367 | ORTHOSTATIC HYPOTENSION |
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 |
|---|---|---|---|---|---|
| 6082367 | 1011144610 | 20081203 | |||
| 6082367 | 1011144611 | 20081203 | |||
| 6082367 | 1011144612 | 20081203 | |||
| 6082367 | 1011144613 | 20081203 |