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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117195647 | 11719564 | 7 | F | 2015 | 20160810 | 20151110 | 20160819 | EXP | CA-PFIZER INC-2015283480 | PFIZER | 21.00 | YR | F | Y | 0.00000 | 20160819 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117195647 | 11719564 | 1 | PS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 2X/DAY | Y | 203214 | 5 | MG | TABLET | BID | |||||
| 117195647 | 11719564 | 2 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 2X/DAY | Y | 203214 | 5 | MG | TABLET | BID | |||||
| 117195647 | 11719564 | 3 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Subcutaneous | 25 MG, WEEKLY | Y | 11719 | 25 | MG | SOLUTION FOR INJECTION | /wk | |||||
| 117195647 | 11719564 | 4 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Subcutaneous | DECREASED DOSE | Y | 11719 | SOLUTION FOR INJECTION | ||||||||
| 117195647 | 11719564 | 5 | SS | PREDNISONE. | PREDNISONE | 1 | 5 MG, DAILY | Y | 0 | 5 | MG | ||||||||
| 117195647 | 11719564 | 6 | SS | LAMICTAL | LAMOTRIGINE | 1 | UNK | Y | 0 | ||||||||||
| 117195647 | 11719564 | 7 | C | CORTISONE | CORTISONEHYDROCORTISONE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 117195647 | 11719564 | 1 | Rheumatoid arthritis |
| 117195647 | 11719564 | 3 | Rheumatoid arthritis |
| 117195647 | 11719564 | 5 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 117195647 | 11719564 | OT |
| 117195647 | 11719564 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117195647 | 11719564 | Abdominal pain | |
| 117195647 | 11719564 | Bronchitis | |
| 117195647 | 11719564 | Clostridium difficile infection | |
| 117195647 | 11719564 | Drug ineffective | |
| 117195647 | 11719564 | Dyspepsia | |
| 117195647 | 11719564 | Dyspnoea | |
| 117195647 | 11719564 | Epilepsy | |
| 117195647 | 11719564 | Nasopharyngitis | |
| 117195647 | 11719564 | Platelet count decreased | |
| 117195647 | 11719564 | Pyrexia | |
| 117195647 | 11719564 | Rash generalised | |
| 117195647 | 11719564 | Rhinorrhoea | |
| 117195647 | 11719564 | Sensitivity to weather change | |
| 117195647 | 11719564 | Sinusitis | |
| 117195647 | 11719564 | White blood cell count 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 |
|---|---|---|---|---|---|---|
| 117195647 | 11719564 | 1 | 20150721 | 20151004 | 0 | |
| 117195647 | 11719564 | 2 | 20151010 | 20151229 | 0 | |
| 117195647 | 11719564 | 3 | 201510 | 0 | ||
| 117195647 | 11719564 | 6 | 20151212 | 0 |