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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125830161 | 12583016 | 1 | I | 201602 | 20160630 | 20160722 | 20160722 | EXP | US-AMGEN-USASP2016087175 | AMGEN | 0.00 | M | Y | 0.00000 | 20160722 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125830161 | 12583016 | 1 | PS | EPOGEN | ERYTHROPOIETIN | 1 | Unknown | UNK | U | 103234 | SOLUTION FOR INJECTION | ||||||||
125830161 | 12583016 | 2 | SS | EPOGEN | ERYTHROPOIETIN | 1 | Unknown | 10000 UNIT, ON MONDAYS, WEDNESDAYS, AND FRIDAYS | U | 103234 | SOLUTION FOR INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125830161 | 12583016 | 1 | Anaemia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125830161 | 12583016 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125830161 | 12583016 | Haemoglobin abnormal |
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 |
---|---|---|---|---|---|---|
125830161 | 12583016 | 2 | 2016 | 0 |