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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125498052 | 12549805 | 2 | F | 20160713 | 20160712 | 20160715 | EXP | KR-BAXTER-2016BAX035703 | BAXTER | 0.00 | F | Y | 0.00000 | 20160715 | CN | KR | KR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125498052 | 12549805 | 1 | PS | EXTRANEAL | CALCIUM CHLORIDEICODEXTRINMAGNESIUM CHLORIDESODIUM CHLORIDESODIUM LACTATE | 1 | Intraperitoneal | 21321 | SOLUTION FOR PERITONEAL DIALYSIS | BID | |||||||||
| 125498052 | 12549805 | 2 | SS | PHYSIONEAL 1.5% | CALCIUM CHLORIDEDEXTROSEMAGNESIUM CHLORIDESODIUM CHLORIDE SOLUTION | 1 | Intraperitoneal | 0 | SOLUTION FOR PERITONEAL DIALYSIS | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125498052 | 12549805 | 1 | End stage renal disease |
| 125498052 | 12549805 | 2 | End stage renal disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125498052 | 12549805 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125498052 | 12549805 | Asthenia | |
| 125498052 | 12549805 | Hypophagia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |