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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126786451 | 12678645 | 1 | I | 20160818 | 20160823 | 20160823 | EXP | CA-AMGEN-CANSP2016108771 | AMGEN | 70.00 | YR | E | F | Y | 0.00000 | 20160823 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126786451 | 12678645 | 1 | PS | ENBREL | ETANERCEPT | 1 | Subcutaneous | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
126786451 | 12678645 | 2 | SS | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Unknown | UNK | 0 | ||||||||||
126786451 | 12678645 | 3 | SS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | UNK | 0 | ||||||||||
126786451 | 12678645 | 4 | SS | DILAUDID | HYDROMORPHONE HYDROCHLORIDE | 1 | Unknown | UNK | 0 | ||||||||||
126786451 | 12678645 | 5 | SS | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | Unknown | UNK | 0 | ||||||||||
126786451 | 12678645 | 6 | SS | METHOTREXATE. | METHOTREXATE | 1 | Subcutaneous | 25 MG,1 EVERY WEEK(S) | 0 | 25 | MG | /wk | |||||||
126786451 | 12678645 | 7 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126786451 | 12678645 | 1 | Rheumatoid arthritis |
126786451 | 12678645 | 2 | Rheumatoid arthritis |
126786451 | 12678645 | 3 | Rheumatoid arthritis |
126786451 | 12678645 | 4 | Rheumatoid arthritis |
126786451 | 12678645 | 5 | Rheumatoid arthritis |
126786451 | 12678645 | 6 | Rheumatoid arthritis |
126786451 | 12678645 | 7 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126786451 | 12678645 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126786451 | 12678645 | Drug ineffective | |
126786451 | 12678645 | Eye disorder | |
126786451 | 12678645 | Fatigue |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |