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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6660962 | 7338912 | I | 6660962-9 | 20100302 | 20100310 | 20100331 | PER | US-BIOGENIDEC-2010BI008228 | BIOGEN IDEC INC. | 66 | YR | F | Y | 20100331 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6660962 | 1013419120 | PS | TYSABRI | 1 | INTRAVENOUS |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6660962 | 1013419120 | MULTIPLE SCLEROSIS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6660962 | FALL |
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 |
---|---|---|---|---|---|
6660962 | 1013419120 | 20100209 |