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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126179331 | 12617933 | 1 | I | 20160105 | 20160727 | 20160803 | 20160803 | EXP | CN-ROCHE-1804168 | ROCHE | 60.00 | YR | M | Y | 60.00000 | KG | 20160803 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126179331 | 12617933 | 1 | PS | ROCEPHIN | CEFTRIAXONE SODIUM | 1 | Intravenous drip | SH1807 | 63239 | 3 | G | QD | |||||||
| 126179331 | 12617933 | 2 | SS | ROCEPHIN | CEFTRIAXONE SODIUM | 1 | Intravenous drip | SH1807 | 63239 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126179331 | 12617933 | 1 | Infection |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126179331 | 12617933 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126179331 | 12617933 | 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 |
|---|---|---|---|---|---|---|
| 126179331 | 12617933 | 1 | 20151229 | 20160105 | 0 | |
| 126179331 | 12617933 | 2 | 20160107 | 20160107 | 0 |