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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8552200 | 8693679 | I | 8552200-7 | 20120719 | 20120720 | 20120731 | PER | US-BIOGENIDEC-2012BI026606 | BIOGEN IDEC INC. | 57 | YR | M | Y | 20120731 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8552200 | 1020397090 | SS | AVONEX | 1 | INTRAMUSCULAR | P41010 | |||||
8552200 | 1020397089 | SS | AVONEX | 1 | INTRAMUSCULAR | ||||||
8552200 | 1020397088 | PS | AVONEX | 1 | INTRAMUSCULAR |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8552200 | 1020397088 | MULTIPLE SCLEROSIS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
8552200 | INJECTION SITE HAEMORRHAGE |
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 |
---|---|---|---|---|---|
8552200 | 1020397090 | 20120719 | |||
8552200 | 1020397089 | 20120719 | |||
8552200 | 1020397088 | 20010430 |