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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127106671 | 12710667 | 1 | I | 2015 | 20160601 | 20160902 | 20160902 | EXP | CA-ORION CORPORATION ORION PHARMA-TREX2016-0421 | ORION | 52.00 | YR | F | Y | 0.00000 | 20160902 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127106671 | 12710667 | 1 | PS | METHOTREXATE (TRADE NAME UNKNOWN) | METHOTREXATE | 1 | Oral | Y | 0 | 15 | MG | /wk | |||||||
127106671 | 12710667 | 2 | SS | METHOTREXATE (TRADE NAME UNKNOWN) | METHOTREXATE | 1 | Oral | Y | 0 | 15 | MG | /wk | |||||||
127106671 | 12710667 | 3 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | Y | 0 | 5 | MG | TABLET | BID | ||||||
127106671 | 12710667 | 4 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | Y | 0 | 5 | MG | TABLET | BID | ||||||
127106671 | 12710667 | 5 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | Y | 0 | 5 | MG | TABLET | BID | ||||||
127106671 | 12710667 | 6 | SS | ATASOL | ACETAMINOPHEN | 1 | Unknown | 0 | |||||||||||
127106671 | 12710667 | 7 | SS | ATASOL | ACETAMINOPHEN | 1 | Unknown | RESUMED | 0 | ||||||||||
127106671 | 12710667 | 8 | SS | NAPROSYN | NAPROXEN | 1 | Unknown | 0 | |||||||||||
127106671 | 12710667 | 9 | SS | NAPROSYN | NAPROXEN | 1 | Unknown | 0 | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127106671 | 12710667 | 1 | Rheumatoid arthritis |
127106671 | 12710667 | 3 | Rheumatoid arthritis |
127106671 | 12710667 | 6 | Pain |
127106671 | 12710667 | 8 | Pain |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127106671 | 12710667 | HO |
127106671 | 12710667 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127106671 | 12710667 | Chromaturia | |
127106671 | 12710667 | Diarrhoea | |
127106671 | 12710667 | Dysuria | |
127106671 | 12710667 | Eye pain | |
127106671 | 12710667 | Fatigue | |
127106671 | 12710667 | Haemorrhoids | |
127106671 | 12710667 | Nail bed bleeding | |
127106671 | 12710667 | Nail infection | |
127106671 | 12710667 | Nasopharyngitis | |
127106671 | 12710667 | Ocular discomfort | |
127106671 | 12710667 | Pollakiuria | |
127106671 | 12710667 | Pyrexia | |
127106671 | 12710667 | Rheumatoid arthritis | |
127106671 | 12710667 | Urinary incontinence | |
127106671 | 12710667 | Urine abnormality | |
127106671 | 12710667 | Uterine cancer | |
127106671 | 12710667 | Vaginal infection | |
127106671 | 12710667 | Vision blurred |
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 |
---|---|---|---|---|---|---|
127106671 | 12710667 | 1 | 20160308 | 0 | ||
127106671 | 12710667 | 2 | 2016 | 0 | ||
127106671 | 12710667 | 3 | 20150821 | 20151104 | 0 | |
127106671 | 12710667 | 4 | 20151109 | 20160315 | 0 | |
127106671 | 12710667 | 5 | 2016 | 0 |