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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4541790 | 5705635 | I | 4541790-7 | 20041216 | 20041216 | 20041230 | EXP | 200414763FR | AVENTIS PHARMACEUTICALS, INC. | M | Y | 20041230 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4541790 | 1005542997 | PS | RILUTEK | 1 | ORAL | ||||||
| 4541790 | 1005542998 | C | TEGELINE | 2 | INTRAVENOUS |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4541790 | 1005542997 | AMYOTROPHIC LATERAL SCLEROSIS |
| 4541790 | 1005542998 | POLYNEUROPATHY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4541790 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4541790 | THROMBOCYTOPENIA |
| 4541790 | WHITE BLOOD CELL COUNT DECREASED |
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 |
|---|---|---|---|---|---|
| 4541790 | 1005542997 | 20040801 | 20041201 | ||
| 4541790 | 1005542998 | 20041213 | 20041215 |