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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123621142 | 12362114 | 2 | F | 201509 | 20160707 | 20160512 | 20160719 | EXP | CA-PFIZER INC-2016245736 | PFIZER | 60.00 | YR | F | Y | 0.00000 | 20160719 | CN | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123621142 | 12362114 | 1 | PS | GABAPENTIN. | GABAPENTIN | 1 | Oral | UNK | 20235 | ||||||||||
| 123621142 | 12362114 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 20 MG, WEEKLY | 11719 | 20 | MG | /wk | |||||||
| 123621142 | 12362114 | 3 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 25 MG, WEEKLY | 11719 | 25 | MG | /wk | |||||||
| 123621142 | 12362114 | 4 | C | PREDNISONE. | PREDNISONE | 1 | UNK | 0 | |||||||||||
| 123621142 | 12362114 | 5 | C | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | Oral | UNK | 0 | ||||||||||
| 123621142 | 12362114 | 6 | C | NAPROSYN | NAPROXEN | 1 | Oral | UNK | 0 | ||||||||||
| 123621142 | 12362114 | 7 | C | MULTIVITAMINS | VITAMINS | 1 | Oral | UNK | 0 | ||||||||||
| 123621142 | 12362114 | 8 | C | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 2X/DAY | 0 | 5 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123621142 | 12362114 | 2 | Rheumatoid arthritis |
| 123621142 | 12362114 | 8 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123621142 | 12362114 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123621142 | 12362114 | Arthritis | |
| 123621142 | 12362114 | Condition aggravated | |
| 123621142 | 12362114 | Drug ineffective | |
| 123621142 | 12362114 | Fall | |
| 123621142 | 12362114 | Humerus fracture | |
| 123621142 | 12362114 | Joint range of motion decreased |
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 |
|---|---|---|---|---|---|---|
| 123621142 | 12362114 | 2 | 20120718 | 20130115 | 0 | |
| 123621142 | 12362114 | 3 | 20160308 | 0 | ||
| 123621142 | 12362114 | 8 | 20160617 | 0 |