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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125555781 | 12555578 | 1 | I | 20160706 | 0 | 20160713 | 20160713 | DIR | 72.00 | YR | F | N | 130.00000 | LBS | 20160708 | Y | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125555781 | 12555578 | 1 | PS | LACTULOSE. | LACTULOSE | 1 | Oral | 1 PACKET ONCE TAKEN BY MOUTH | D | 27S161035 | 20180801 | 0 | 1 | DF | 1X | ||||
| 125555781 | 12555578 | 2 | SS | SIBO, 10 G | DEVICE | 1 | 27S161035 | 0 | |||||||||||
| 125555781 | 12555578 | 4 | C | LUMINGAN | 2 | 0 | |||||||||||||
| 125555781 | 12555578 | 5 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125555781 | 12555578 | 1 | Laboratory test |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125555781 | 12555578 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125555781 | 12555578 | Dehydration | |
| 125555781 | 12555578 | Diarrhoea | |
| 125555781 | 12555578 | Product label issue |
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 |
|---|---|---|---|---|---|---|
| 125555781 | 12555578 | 1 | 20160706 | 20160706 | 0 |