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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8480324 | 8644630 | I | 8480324-1 | 20110101 | 20120619 | 20120630 | EXP | JP-AMGEN-JPNSP2012039055 | AMGENSAFETY | YR | F | Y | 20120630 | CN | JAPAN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8480324 | 1020135209 | PS | ENBREL | 1 | SUBCUTANEOUS | UNK | |||||
8480324 | 1020135210 | SS | RHEUMATREX | 1 | ORAL | UNK |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8480324 | 1020135209 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
8480324 | OT |
Reactions reported
Event ID | PT |
---|---|
8480324 | BLOOD CHOLESTEROL INCREASED |
8480324 | AGE-RELATED MACULAR DEGENERATION |
8480324 | EPISTAXIS |
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 |
---|---|---|---|---|---|
8480324 | 1020135209 | 20060601 |