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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127313581 | 12731358 | 1 | I | 20160314 | 0 | 20160909 | 20160909 | DIR | US-FDA-350156 | FDA-CTU | 5.34 | YR | M | N | 21.00000 | KG | 20160909 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127313581 | 12731358 | 1 | PS | DOCUSATE LIQUID | DOCUSATE | 1 | Oral | D | D | 0 | 52.5 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127313581 | 12731358 | 1 | Constipation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127313581 | 12731358 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127313581 | 12731358 | Burkholderia test positive | |
| 127313581 | 12731358 | Cerebral haemorrhage | |
| 127313581 | 12731358 | Fall | |
| 127313581 | 12731358 | Renal failure | |
| 127313581 | 12731358 | Septic shock | |
| 127313581 | 12731358 | Weaning failure |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | CASEID | RPSR COD |
|---|---|---|
| 127313581 | 12731358 | HP |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 127313581 | 12731358 | 1 | 20160314 | 20160507 | 0 |