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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542775 | 5706515 | I | 4542775-7 | 20041216 | 20041220 | 20041231 | EXP | 200419814US | AVENTIS PHARMACEUTICALS, INC. | F | Y | 20041231 | OT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542775 | 1005546847 | PS | DOCETAXEL | 2 | DOSE: UNK | UNK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4542775 | 1005546847 | OESOPHAGEAL CARCINOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4542775 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4542775 | CHYLOTHORAX |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4542775 | HP |
Therapies reported
| no results found |