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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7581964 | 7917479 | F | 7581964-4 | 20110220 | 20110622 | 20110630 | EXP | US-BIOGENIDEC-2011BI015099 | BIOGEN IDEC INC. | 27 | YR | F | Y | 20110630 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7581964 | 1016899632 | PS | TYSABRI | 1 | INTRAVENOUS |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7581964 | 1016899632 | MULTIPLE SCLEROSIS |
Outcome of event
Event ID | OUTC COD |
---|---|
7581964 | HO |
Reactions reported
Event ID | PT |
---|---|
7581964 | PANCREATITIS |
7581964 | CHOLECYSTITIS |
7581964 | MULTIPLE SCLEROSIS RELAPSE |
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 |
---|---|---|---|---|---|
7581964 | 1016899632 | 20081208 |