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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127219611 | 12721961 | 1 | I | 20160730 | 20160826 | 20160907 | 20160907 | EXP | DE-TEVA-688995GER | TEVA | 4.00 | YR | M | Y | 19.00000 | KG | 20160907 | MD | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127219611 | 12721961 | 1 | PS | PROPOFOL. | PROPOFOL | 1 | Intravenous (not otherwise specified) | 75102 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127219611 | 12721961 | 1 | Medical induction of coma |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127219611 | 12721961 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127219611 | 12721961 | Arrhythmia | |
| 127219611 | 12721961 | Blood triglycerides increased | |
| 127219611 | 12721961 | Lactic acidosis | |
| 127219611 | 12721961 | Propofol infusion syndrome | |
| 127219611 | 12721961 | Renal failure | |
| 127219611 | 12721961 | Rhabdomyolysis |
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 |
|---|---|---|---|---|---|---|
| 127219611 | 12721961 | 1 | 20160727 | 20160730 | 0 |