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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125234781 | 12523478 | 1 | I | 20151113 | 20160623 | 20160703 | 20160703 | EXP | CN-BAXTER-2016BAX033912 | BAXTER | 80.27 | YR | F | Y | 55.00000 | KG | 20160703 | MD | CN | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125234781 | 12523478 | 1 | PS | 0.9% SODIUM CHLORIDE INJECTION | SODIUM CHLORIDE | 1 | Intravenous drip | Y | S1406118 | 16677 | 100 | ML | INJECTION | QID | |||||
| 125234781 | 12523478 | 2 | SS | VANCOMYCIN | VANCOMYCIN | 1 | Intravenous drip | Y | C204371 | 0 | 500 | MG | INJECTION | QID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125234781 | 12523478 | 1 | Medication dilution |
| 125234781 | 12523478 | 2 | Infection |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125234781 | 12523478 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125234781 | 12523478 | Deafness unilateral | |
| 125234781 | 12523478 | Pyrexia |
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 |
|---|---|---|---|---|---|---|
| 125234781 | 12523478 | 1 | 20151108 | 20151113 | 0 | |
| 125234781 | 12523478 | 2 | 20151108 | 20151113 | 0 |