Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126118731 | 12611873 | 1 | I | 20150101 | 20151014 | 20160801 | 20160801 | PER | US-PFIZER INC-3054997 | PFIZER | 46.00 | YR | F | Y | 0.00000 | 20160801 | CN | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126118731 | 12611873 | 1 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | UNK | Y | UNK | 11719 | ||||||||
| 126118731 | 12611873 | 2 | SS | ETANERCEPT | ETANERCEPT | 1 | Unknown | FREQ: 1 WEEK; INTERVAL: 1 | UNK | 0 | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126118731 | 12611873 | 1 | Rheumatoid arthritis |
| 126118731 | 12611873 | 2 | Rheumatoid arthritis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126118731 | 12611873 | Alopecia | |
| 126118731 | 12611873 | Drug effect incomplete | |
| 126118731 | 12611873 | Headache | |
| 126118731 | 12611873 | Nausea | |
| 126118731 | 12611873 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 126118731 | 12611873 | 1 | 20150701 | 0 | ||
| 126118731 | 12611873 | 2 | 20150701 | 0 |