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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126047761 | 12604776 | 1 | I | 20160711 | 20160725 | 20160728 | 20160728 | EXP | PA-ABBVIE-16P-125-1686238-00 | ABBVIE | 42.58 | YR | F | Y | 0.00000 | 20160728 | CN | COUNTRY NOT SPECIFIED | PA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126047761 | 12604776 | 1 | PS | ZEMPLAR | PARICALCITOL | 1 | Intravenous (not otherwise specified) | ZEMPLAR WAS ADMINISTERED DURING HEMODIALYSIS | UNKNOWN | 20819 | .25 | UG | SOLUTION FOR INJECTION | TIW |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126047761 | 12604776 | 1 | Hyperparathyroidism secondary |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126047761 | 12604776 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126047761 | 12604776 | Death |
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 |
---|---|---|---|---|---|---|
126047761 | 12604776 | 1 | 20130111 | 0 |