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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126537041 | 12653704 | 1 | I | 201607 | 20160809 | 20160816 | 20160816 | EXP | US-AMGEN-USASP2016104088 | AMGEN | 74.00 | YR | E | F | Y | 0.00000 | 20160815 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126537041 | 12653704 | 1 | PS | PROLIA | DENOSUMAB | 1 | Unknown | UNK UNK, Q6MO | U | 125320 | SOLUTION FOR INJECTION | ||||||||
126537041 | 12653704 | 2 | SS | ENBREL | ETANERCEPT | 1 | Unknown | UNK UNK, Q2WK | Y | 0 | UNKNOWN FORMULATION | QOW |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126537041 | 12653704 | 1 | Osteoporosis postmenopausal |
126537041 | 12653704 | 2 | Vasculitis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126537041 | 12653704 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126537041 | 12653704 | Cellulitis | |
126537041 | 12653704 | Immunosuppression | |
126537041 | 12653704 | Limb discomfort | |
126537041 | 12653704 | Musculoskeletal discomfort | |
126537041 | 12653704 | Off label use |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |