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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126635701 | 12663570 | 1 | I | 20160711 | 20160815 | 20160818 | 20160818 | EXP | VE-ABBVIE-16P-178-1703449-00 | ABBVIE | 50.13 | YR | F | Y | 0.00000 | 20160818 | OT | COUNTRY NOT SPECIFIED | VE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126635701 | 12663570 | 1 | PS | ZEMPLAR | PARICALCITOL | 1 | Intravenous (not otherwise specified) | UNKNOWN | 20819 | INJECTION | |||||||||
| 126635701 | 12663570 | 2 | C | OLMESARTAN | OLMESARTAN | 1 | 0 | ||||||||||||
| 126635701 | 12663570 | 3 | C | HEPARIN | HEPARIN SODIUM | 1 | 0 | ||||||||||||
| 126635701 | 12663570 | 4 | C | ERYTHROPOIETIN | ERYTHROPOIETIN | 1 | 0 | ||||||||||||
| 126635701 | 12663570 | 5 | C | FOLIC ACID. | FOLIC ACID | 1 | 0 | ||||||||||||
| 126635701 | 12663570 | 6 | C | BENUTREX | 2 | 0 | |||||||||||||
| 126635701 | 12663570 | 7 | C | JANUMET | METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126635701 | 12663570 | 1 | Product used for unknown indication |
| 126635701 | 12663570 | 2 | Product used for unknown indication |
| 126635701 | 12663570 | 3 | Product used for unknown indication |
| 126635701 | 12663570 | 4 | Product used for unknown indication |
| 126635701 | 12663570 | 5 | Product used for unknown indication |
| 126635701 | 12663570 | 6 | Product used for unknown indication |
| 126635701 | 12663570 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126635701 | 12663570 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126635701 | 12663570 | Cerebrovascular disorder |
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 |
|---|---|---|---|---|---|---|
| 126635701 | 12663570 | 1 | 20160212 | 0 |