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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126846902 | 12684690 | 2 | F | 20160826 | 20160825 | 20160826 | EXP | CA-PFIZER INC-2016400412 | PFIZER | 70.00 | YR | F | Y | 0.00000 | 20160826 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126846902 | 12684690 | 1 | SS | ENBREL | ETANERCEPT | 1 | Subcutaneous | UNK | U | 0 | |||||||||
126846902 | 12684690 | 2 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Subcutaneous | 25 MG,1 EVERY WEEK(S) | U | 11719 | 25 | MG | SOLUTION FOR INJECTION | /wk | |||||
126846902 | 12684690 | 3 | SS | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | UNK | U | 0 | ||||||||||
126846902 | 12684690 | 4 | SS | ACTEMRA | TOCILIZUMAB | 1 | UNK | U | 0 | ||||||||||
126846902 | 12684690 | 5 | SS | DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
126846902 | 12684690 | 6 | SS | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | UNK | U | 0 | ||||||||||
126846902 | 12684690 | 7 | SS | PREDNISONE. | PREDNISONE | 1 | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126846902 | 12684690 | 1 | Rheumatoid arthritis |
126846902 | 12684690 | 2 | Rheumatoid arthritis |
126846902 | 12684690 | 3 | Rheumatoid arthritis |
126846902 | 12684690 | 4 | Rheumatoid arthritis |
126846902 | 12684690 | 5 | Rheumatoid arthritis |
126846902 | 12684690 | 6 | Rheumatoid arthritis |
126846902 | 12684690 | 7 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126846902 | 12684690 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126846902 | 12684690 | Drug ineffective | |
126846902 | 12684690 | Eye disorder | |
126846902 | 12684690 | Fatigue |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |