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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7788003 | 7683465 | I | 7788003-0 | 20090701 | 20090907 | 20110930 | PER | 2009BI028644 | BIOGEN IDEC INC. | 45 | YR | M | Y | 20110930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7788003 | 1017673653 | PS | TYSABRI | 1 | INTRAVENOUS |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7788003 | 1017673653 | MULTIPLE SCLEROSIS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
7788003 | ASTHENIA |
7788003 | MUSCULAR WEAKNESS |
7788003 | BALANCE DISORDER |
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 |
---|---|---|---|---|---|
7788003 | 1017673653 | 20090727 |