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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126603411 | 12660341 | 1 | I | 20160310 | 20160810 | 20160817 | 20160817 | EXP | CN-PFIZER INC-2016389001 | PFIZER | 49.00 | YR | F | Y | 65.00000 | KG | 20160817 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126603411 | 12660341 | 1 | PS | SOLU-MEDROL | METHYLPREDNISOLONE SODIUM SUCCINATE | 1 | Intravenous (not otherwise specified) | 20 MG, 1X/DAY | 40 | MG | Y | L90165 | 11856 | 20 | MG | POWDER FOR SOLUTION FOR INJECTION | QD | ||
126603411 | 12660341 | 2 | SS | SOLU-MEDROL | METHYLPREDNISOLONE SODIUM SUCCINATE | 1 | Intravenous (not otherwise specified) | 20 MG, 1X/DAY | 40 | MG | Y | 11856 | 20 | MG | POWDER FOR SOLUTION FOR INJECTION | QD | |||
126603411 | 12660341 | 3 | SS | SOLU-MEDROL | METHYLPREDNISOLONE SODIUM SUCCINATE | 1 | Intravenous (not otherwise specified) | 20 MG, 1X/DAY | 40 | MG | Y | 11856 | 20 | MG | POWDER FOR SOLUTION FOR INJECTION | QD | |||
126603411 | 12660341 | 4 | SS | PIPERACILLIN AND TAZOBACTAM | PIPERACILLIN SODIUMTAZOBACTAM SODIUM | 1 | Intravenous drip | 3.375 G, 3X/DAY | 30 | G | Y | 151001 | 0 | 3.375 | G | POWDER FOR INJECTION | TID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126603411 | 12660341 | 1 | Infection |
126603411 | 12660341 | 4 | Infection |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126603411 | 12660341 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126603411 | 12660341 | Hepatocellular injury |
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 |
---|---|---|---|---|---|---|
126603411 | 12660341 | 1 | 20160305 | 20160305 | 0 | |
126603411 | 12660341 | 2 | 20160306 | 20160306 | 0 | |
126603411 | 12660341 | 3 | 20160312 | 20160312 | 0 | |
126603411 | 12660341 | 4 | 20160308 | 20160310 | 0 |