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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7914836 | 8245044 | I | 7914836-3 | 20101201 | 20111107 | 20111115 | EXP | US-AMGEN-USASP2011058240 | AMGENSAFETY | 62 | YR | F | Y | 20111115 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7914836 | 1018049378 | PS | ENBREL | 1 | 50 MG, QWK | ||||||
7914836 | 1018049380 | C | METHOTREXATE | 1 | 1 MG, UNK | ||||||
7914836 | 1018049379 | SS | ENBREL | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7914836 | 1018049378 | PSORIATIC ARTHROPATHY |
7914836 | 1018049379 | PSORIASIS |
Outcome of event
Event ID | OUTC COD |
---|---|
7914836 | HO |
Reactions reported
Event ID | PT |
---|---|
7914836 | DYSPHAGIA |
7914836 | LOSS OF CONSCIOUSNESS |
7914836 | DIARRHOEA |
7914836 | DEHYDRATION |
7914836 | CONTUSION |
7914836 | DISTURBANCE IN ATTENTION |
7914836 | PSORIATIC ARTHROPATHY |
7914836 | RECTOCELE |
7914836 | CYSTOCELE |
7914836 | PERIORBITAL HAEMATOMA |
7914836 | PSORIASIS |
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 |
---|---|---|---|---|---|
7914836 | 1018049378 | 20091113 | 20100901 | ||
7914836 | 1018049380 | 20040101 |