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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4626842 | 5774031 | I | 4626842-5 | 20050210 | 20050317 | 20050331 | EXP | 2005BI006059 | BIOGEN IDEC INC. | F | N | 20050330 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4626842 | 1005846414 | PS | NATALIZUMAB | 2 | INTRAVENOUS | 300 MG; QM; IV | D | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4626842 | 1005846414 | MULTIPLE SCLEROSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4626842 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4626842 | BLOOD PRESSURE DECREASED |
| 4626842 | HYPERSENSITIVITY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4626842 | CSM |
| 4626842 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4626842 | 1005846414 | 20050101 | 20050210 |