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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124797914 | 12479791 | 4 | F | 20160720 | 20160620 | 20160725 | PER | US-PFIZER INC-2016304660 | PFIZER | 64.00 | YR | F | Y | 0.00000 | 20160725 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124797914 | 12479791 | 1 | SS | ENBREL | ETANERCEPT | 1 | UNK | U | 0 | ||||||||||
124797914 | 12479791 | 2 | PS | MEDROL | METHYLPREDNISOLONE | 1 | UNK | U | 11153 | TABLET | |||||||||
124797914 | 12479791 | 3 | SS | CELEBREX | CELECOXIB | 1 | Oral | 200 MG, 1X/DAY | U | 20998 | 200 | MG | CAPSULE, HARD | QD | |||||
124797914 | 12479791 | 4 | SS | CELEBREX | CELECOXIB | 1 | U | 20998 | CAPSULE, HARD | ||||||||||
124797914 | 12479791 | 5 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 17.5 MG, WEEKLY (2.5 MG TABLET TAKE 7 TABLETS A WEEK) | 11719 | 17.5 | MG | /wk | |||||||
124797914 | 12479791 | 6 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 15.0 MG, WEEKLY (2.5 MG TABLET TAKE 6 TABLETS A WEEK) | 11719 | 15 | MG | /wk | |||||||
124797914 | 12479791 | 7 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 7.5 MG, WEEKLY (2.5 MG TABLET TAKE 3 TABLETS WEEK) | 11719 | 7.5 | MG | /wk | |||||||
124797914 | 12479791 | 8 | SS | TRAMADOL. | TRAMADOL | 1 | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124797914 | 12479791 | 1 | Rheumatoid arthritis |
124797914 | 12479791 | 2 | Rheumatoid arthritis |
124797914 | 12479791 | 3 | Rheumatoid arthritis |
124797914 | 12479791 | 4 | Antiinflammatory therapy |
124797914 | 12479791 | 5 | Rheumatoid arthritis |
124797914 | 12479791 | 8 | Rheumatoid arthritis |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124797914 | 12479791 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |