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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6452467 | 7186083 | I | 6452467-5 | 20070625 | 20090209 | 20091123 | PER | US-AMGEN-KDL332975 | AMGENSAFETY | 63 | F | Y | 20091123 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6452467 | 1012630615 | PS | ENBREL | 1 | SUBCUTANEOUS | 1006771 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6452467 | 1012630615 | RHEUMATOID ARTHRITIS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6452467 | INJECTION SITE PAIN |
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 |
---|---|---|---|---|---|
6452467 | 1012630615 | 20070625 |