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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
120780934 | 12078093 | 4 | F | 201411 | 20160715 | 20160215 | 20160725 | EXP | CA-PFIZER INC-2014304761 | PFIZER | 52.00 | YR | F | Y | 0.00000 | 20160725 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
120780934 | 12078093 | 1 | PS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 2X/DAY | Y | 203214 | 5 | MG | TABLET | BID | |||||
120780934 | 12078093 | 2 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 2X/DAY | Y | 203214 | 5 | MG | TABLET | BID | |||||
120780934 | 12078093 | 3 | SS | PREDNISONE. | PREDNISONE | 1 | Oral | 15 MG, DAILY | 0 | 15 | MG | ||||||||
120780934 | 12078093 | 4 | C | TYLENOL | ACETAMINOPHEN | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
120780934 | 12078093 | 1 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
120780934 | 12078093 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
120780934 | 12078093 | Bone pain | |
120780934 | 12078093 | Condition aggravated | |
120780934 | 12078093 | Diarrhoea | |
120780934 | 12078093 | Disease recurrence | |
120780934 | 12078093 | Headache | |
120780934 | 12078093 | Oral candidiasis | |
120780934 | 12078093 | Pain | |
120780934 | 12078093 | Rheumatoid arthritis | |
120780934 | 12078093 | Tooth disorder | |
120780934 | 12078093 | Upper respiratory tract infection | |
120780934 | 12078093 | Vulval cancer | |
120780934 | 12078093 | Vulvovaginal burning sensation | |
120780934 | 12078093 | Vulvovaginal disorder | |
120780934 | 12078093 | Vulvovaginal dryness | |
120780934 | 12078093 | Vulvovaginal pain | |
120780934 | 12078093 | Vulvovaginal swelling |
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 |
---|---|---|---|---|---|---|
120780934 | 12078093 | 1 | 20141010 | 20141103 | 0 |