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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127295841 | 12729584 | 1 | I | 20160825 | 0 | 20160907 | 20160907 | DIR | FDA-CTU | 52.00 | YR | M | N | 102.60000 | KG | 20160907 | N | PH | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127295841 | 12729584 | 1 | PS | CEFTRIAXONE. | CEFTRIAXONE | 1 | Intravenous (not otherwise specified) | Y | D | 0 | 2 | G | 1X | ||||||
127295841 | 12729584 | 2 | SS | MEROPENEM. | MEROPENEM | 1 | Intravenous (not otherwise specified) | Y | D | 0 | 1000 | MG | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127295841 | 12729584 | 1 | Pneumonia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127295841 | 12729584 | HO |
127295841 | 12729584 | RI |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127295841 | 12729584 | Acute kidney injury | |
127295841 | 12729584 | Arthralgia | |
127295841 | 12729584 | Myalgia | |
127295841 | 12729584 | Rash |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | CASEID | RPSR COD |
---|---|---|
127295841 | 12729584 | HP |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
127295841 | 12729584 | 1 | 20160811 | 20160812 | 0 | |
127295841 | 12729584 | 2 | 20160814 | 20160818 | 0 |