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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127205981 | 12720598 | 1 | I | 20160730 | 20160829 | 20160907 | 20160907 | EXP | DE-PFIZER INC-2016408050 | PFIZER | 4.00 | YR | M | Y | 0.00000 | 20160907 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127205981 | 12720598 | 1 | PS | PROPOFOL. | PROPOFOL | 1 | Intravenous (not otherwise specified) | UNK | 77908 | EMULSION FOR INJECTION |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127205981 | 12720598 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127205981 | 12720598 | Arrhythmia | |
127205981 | 12720598 | Blood triglycerides increased | |
127205981 | 12720598 | Lactic acidosis | |
127205981 | 12720598 | Propofol infusion syndrome | |
127205981 | 12720598 | Renal failure | |
127205981 | 12720598 | 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 |
---|---|---|---|---|---|---|
127205981 | 12720598 | 1 | 20160727 | 20160730 | 0 |