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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5375459 | 6346329 | I | 5375459-6 | 20070420 | 20070615 | 20070629 | EXP | CA-SHR-CA-2007-022592 | BERLEX | 65 | YR | M | Y | 20070629 | 20070420 | CANADA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5375459 | 1008649600 | PS | BETASERON | 1 | SUBCUTANEOUS | 8 MIU, EVERY 2D |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5375459 | 1008649600 | SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS |
Outcome of event
Event ID | OUTC COD |
---|---|
5375459 | DE |
Reactions reported
Event ID | PT |
---|---|
5375459 | DEATH |
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 |
---|---|---|---|---|---|
5375459 | 1008649600 | 20000508 | 20070420 | 2538 | DAY |