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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4541789 | 5705634 | I | 4541789-0 | 20031110 | 20041215 | 20041230 | EXP | 200413969JP | AVENTIS PHARMACEUTICALS, INC. | 62 | YR | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4541789 | 1005542996 | PS | RILUTEK | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4541789 | 1005542996 | AMYOTROPHIC LATERAL SCLEROSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4541789 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4541789 | COUGH |
| 4541789 | DYSPNOEA |
| 4541789 | LYMPHOCYTE STIMULATION TEST POSITIVE |
| 4541789 | PNEUMONIA |
| 4541789 | PULMONARY TOXICITY |
| 4541789 | PYREXIA |
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 |
|---|---|---|---|---|---|
| 4541789 | 1005542996 | 20031020 |