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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7205253 | 7745019 | I | 7205253-2 | 20100101 | 20101221 | 20101231 | PER | US-BIOGENIDEC-2010BI045044 | BIOGEN IDEC INC. | 52 | YR | F | Y | 20101231 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7205253 | 1015448399 | PS | TYSABRI | 1 | INTRAVENOUS | ||||||
| 7205253 | 1015448400 | C | AMPYRA | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7205253 | 1015448399 | MULTIPLE SCLEROSIS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 7205253 | BACK PAIN |
| 7205253 | CLONUS |
| 7205253 | FATIGUE |
| 7205253 | LHERMITTE'S SIGN |
| 7205253 | MOBILITY DECREASED |
| 7205253 | NAUSEA |
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 |
|---|---|---|---|---|---|
| 7205253 | 1015448399 | 20100319 | |||
| 7205253 | 1015448400 | 20100601 | 20101101 |