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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
119666542 | 11966654 | 2 | F | 20160121 | 20160817 | 20160127 | 20160822 | EXP | CA-AMGEN-CANSP2012046460 | AMGEN | 46.00 | YR | A | F | Y | 0.00000 | 20160822 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
119666542 | 11966654 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | 50 MG, QWK | U | 103795 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk | |||||
119666542 | 11966654 | 2 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Unknown | UNK | 0 | ||||||||||
119666542 | 11966654 | 3 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | UNK | 0 | ||||||||||
119666542 | 11966654 | 4 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | UNK | 0 | TABLET | |||||||||
119666542 | 11966654 | 5 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | UNK | 0 | TABLET | |||||||||
119666542 | 11966654 | 6 | C | NAPROXEN. | NAPROXEN | 1 | UNK | 0 | |||||||||||
119666542 | 11966654 | 7 | C | MEFENAMIC ACID. | MEFENAMIC ACID | 1 | UNK UNK, AS NECESSARY | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
119666542 | 11966654 | 1 | Rheumatoid arthritis |
119666542 | 11966654 | 2 | Rheumatoid arthritis |
119666542 | 11966654 | 3 | Rheumatoid arthritis |
119666542 | 11966654 | 4 | Rheumatoid arthritis |
119666542 | 11966654 | 5 | Rheumatoid arthritis |
119666542 | 11966654 | 6 | Pain |
119666542 | 11966654 | 7 | Pain |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
119666542 | 11966654 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
119666542 | 11966654 | Alopecia totalis | |
119666542 | 11966654 | Alopecia universalis | |
119666542 | 11966654 | Condition aggravated | |
119666542 | 11966654 | Drug effect decreased | |
119666542 | 11966654 | Drug ineffective | |
119666542 | 11966654 | Ear infection | |
119666542 | 11966654 | Herpes zoster | |
119666542 | 11966654 | Pain | |
119666542 | 11966654 | Sinusitis |
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 |
---|---|---|---|---|---|---|
119666542 | 11966654 | 1 | 20090525 | 0 |