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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126183681 | 12618368 | 1 | I | 2015 | 20160315 | 20160803 | 20160803 | PER | US-PFIZER INC-2016162141 | PFIZER | 47.00 | YR | M | Y | 0.00000 | 20160803 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126183681 | 12618368 | 1 | SS | ENBREL | ETANERCEPT | 1 | 50 MG, UNK | 0 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | ||||||||
126183681 | 12618368 | 2 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | 2.5 MG, FREQ: 6 WEEK; INTERVAL: 1 | 11719 | 2.5 | MG | |||||||||
126183681 | 12618368 | 3 | SS | NAPROXEN. | NAPROXEN | 1 | UNK | 0 | |||||||||||
126183681 | 12618368 | 4 | SS | HUMIRA | ADALIMUMAB | 1 | 40 MG, UNK | 0 | 40 | MG | |||||||||
126183681 | 12618368 | 5 | C | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 2X/DAY | 0 | 5 | MG | TABLET | BID | ||||||
126183681 | 12618368 | 6 | C | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, UNK (FREQ: 2 DAY; INTERVAL: 1) | 0 | 5 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126183681 | 12618368 | 1 | Rheumatoid arthritis |
126183681 | 12618368 | 2 | Rheumatoid arthritis |
126183681 | 12618368 | 3 | Rheumatoid arthritis |
126183681 | 12618368 | 4 | Rheumatoid arthritis |
126183681 | 12618368 | 5 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126183681 | 12618368 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126183681 | 12618368 | Drug ineffective |
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 |
---|---|---|---|---|---|---|
126183681 | 12618368 | 1 | 20160101 | 0 | ||
126183681 | 12618368 | 2 | 20160101 | 0 | ||
126183681 | 12618368 | 3 | 20160301 | 0 | ||
126183681 | 12618368 | 4 | 20150701 | 20150801 | 0 |