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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6918423 | 7536299 | I | 6918423-5 | 20100806 | 20100806 | 20100811 | PER | US-BIOGENIDEC-2010BI027279 | BIOGEN IDEC INC. | 32 | YR | F | Y | 20100811 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6918423 | 1014389593 | PS | TYSABRI | 1 | INTRAVENOUS | ||||||
| 6918423 | 1014389594 | SS | TYSABRI | 1 | INTRAVENOUS |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6918423 | 1014389593 | MULTIPLE SCLEROSIS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6918423 | FATIGUE |
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 |
|---|---|---|---|---|---|
| 6918423 | 1014389593 | 20050215 | 20050201 | ||
| 6918423 | 1014389594 | 20090805 |