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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124968482 | 12496848 | 2 | F | 20151001 | 20160921 | 20160624 | 20160923 | EXP | VE-ABBVIE-16P-178-1660737-00 | ABBVIE | 15.45 | YR | M | Y | 0.00000 | 20160923 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124968482 | 12496848 | 1 | PS | ZEMPLAR | PARICALCITOL | 1 | Unknown | N | 457508E02 | 21606 | |||||||||
| 124968482 | 12496848 | 2 | SS | ZEMPLAR | PARICALCITOL | 1 | Unknown | N | 457508E02 | 21606 | |||||||||
| 124968482 | 12496848 | 3 | C | FOLIC ACID. | FOLIC ACID | 1 | 0 | ||||||||||||
| 124968482 | 12496848 | 4 | C | IRON | IRON | 1 | 0 | ||||||||||||
| 124968482 | 12496848 | 5 | C | CALCIUM ACETATE. | CALCIUM ACETATE | 1 | 0 | ||||||||||||
| 124968482 | 12496848 | 6 | C | ERYTHROPOIETIN | ERYTHROPOIETIN | 1 | 0 | ||||||||||||
| 124968482 | 12496848 | 7 | C | BENUTREX | 2 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124968482 | 12496848 | 1 | Product used for unknown indication |
| 124968482 | 12496848 | 3 | Product used for unknown indication |
| 124968482 | 12496848 | 4 | Product used for unknown indication |
| 124968482 | 12496848 | 5 | Product used for unknown indication |
| 124968482 | 12496848 | 6 | Product used for unknown indication |
| 124968482 | 12496848 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124968482 | 12496848 | HO |
| 124968482 | 12496848 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124968482 | 12496848 | Acute pulmonary oedema | |
| 124968482 | 12496848 | Cardiac failure | |
| 124968482 | 12496848 | Catheter site discharge | |
| 124968482 | 12496848 | Dyspnoea | |
| 124968482 | 12496848 | Fluid overload | |
| 124968482 | 12496848 | General physical health deterioration | |
| 124968482 | 12496848 | Mucosal discolouration | |
| 124968482 | 12496848 | Respiratory distress | |
| 124968482 | 12496848 | Seizure | |
| 124968482 | 12496848 | Underweight | |
| 124968482 | 12496848 | Uraemic encephalopathy |
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 |
|---|---|---|---|---|---|---|
| 124968482 | 12496848 | 1 | 20160524 | 0 | ||
| 124968482 | 12496848 | 2 | 20131210 | 20160531 | 0 |