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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125228801 | 12522880 | 1 | I | 20160604 | 20160630 | 20160701 | 20160701 | EXP | CO-ABBVIE-16P-036-1667390-00 | ABBVIE | 56.59 | YR | F | Y | 0.00000 | 20160701 | CN | COUNTRY NOT SPECIFIED | CO |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125228801 | 12522880 | 1 | PS | ZEMPLAR | PARICALCITOL | 1 | Oral | UNKNOWN | 21606 | 1 | UG | CAPSULE | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125228801 | 12522880 | 1 | Hyperparathyroidism secondary |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125228801 | 12522880 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125228801 | 12522880 | Myocardial infarction |
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 |
---|---|---|---|---|---|---|
125228801 | 12522880 | 1 | 20160405 | 20160604 | 0 |