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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8024929 | 8716001 | I | 8024929-0 | 20111219 | 20111222 | 20120103 | EXP | ACO_28606_2011 | ACORDA THHERAPEUTICS, INC. | 40 | YR | M | N | 20111230 | CN | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8024929 | 1018452762 | PS | FAMPYRA (DALFAMPRIDINE) TABLET, 10MG | 2 | ORAL | 10 MG, BID, ORAL | D | D | 22250 | ||
| 8024929 | 1018491013 | C | AVONEX | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8024929 | 1018452762 | MULTIPLE SCLEROSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8024929 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 8024929 | FEMORAL NECK FRACTURE |
| 8024929 | BALANCE DISORDER |
| 8024929 | FALL |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 8024929 | CSM |
| 8024929 | FGN |
| 8024929 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 8024929 | 1018452762 | 20111008 |