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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8480329 | 8439903 | F | 8480329-0 | 20110601 | 20120621 | 20120630 | EXP | DK-TEVA-324463ISR | TEVA | 61 | YR | F | Y | 88 | KG | 20120630 | MD | DENMARK |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8480329 | 1020135229 | C | FOLIC ACID | 1 | |||||||
8480329 | 1020135228 | SS | HUMIRA | 1 | |||||||
8480329 | 1020135227 | PS | METHOTREXATE | 1 | ORAL | 081099 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8480329 | 1020135228 | PSORIATIC ARTHROPATHY |
8480329 | 1020135227 | PSORIATIC ARTHROPATHY |
Outcome of event
Event ID | OUTC COD |
---|---|
8480329 | HO |
Reactions reported
Event ID | PT |
---|---|
8480329 | UTERINE CANCER |
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 |
---|---|---|---|---|---|
8480329 | 1020135228 | 20070430 | 20110523 | ||
8480329 | 1020135227 | 20070403 | 20110405 |