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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6452468 | 7186084 | I | 6452468-7 | 20090201 | 20090209 | 20091123 | PER | US-AMGEN-KDL332997 | AMGENSAFETY | 61 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6452468 | 1012630616 | PS | ENBREL | 1 | SUBCUTANEOUS | UNKNOWN |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6452468 | 1012630616 | RHEUMATOID ARTHRITIS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6452468 | RASH |
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 |
---|---|---|---|---|---|
6452468 | 1012630616 | 20030101 |