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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127957061 | 12795706 | 1 | I | 20150819 | 20160926 | 20160929 | 20160929 | EXP | GB-ASTRAZENECA-2016SF02699 | ASTRAZENECA | 5.00 | YR | F | Y | 15.00000 | KG | 20160929 | MD | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127957061 | 12795706 | 1 | PS | MEROPENEM. | MEROPENEM | 1 | Oral | 1800 | MG | D | 50706 | 150 | MG | SOLUTION FOR INJECTION | TID | ||||
127957061 | 12795706 | 2 | C | CEFOTAXIME | CEFOTAXIME SODIUM | 1 | 0 | ||||||||||||
127957061 | 12795706 | 3 | C | GENTAMICIN. | GENTAMICIN | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127957061 | 12795706 | 1 | Urinary tract infection bacterial |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127957061 | 12795706 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127957061 | 12795706 | Multiple organ dysfunction syndrome | |
127957061 | 12795706 | Pancreatitis acute |
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 |
---|---|---|---|---|---|---|
127957061 | 12795706 | 1 | 20150815 | 20150829 | 0 |