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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125725011 | 12572501 | 1 | I | 2016 | 20160512 | 20160719 | 20160719 | PER | US-BAUSCH-BL-2016-011609 | BAUSCH AND LOMB | 52.71 | YR | F | Y | 0.00000 | 20160719 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125725011 | 12572501 | 1 | PS | XIFAXAN | RIFAXIMIN | 1 | Oral | 21361 | 550 | MG | TABLET | BID | |||||||
| 125725011 | 12572501 | 2 | SS | MONTELUKAST | MONTELUKAST SODIUM | 1 | Oral | 0 | |||||||||||
| 125725011 | 12572501 | 3 | SS | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | Oral | 0 | 100 | MG | |||||||||
| 125725011 | 12572501 | 4 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | 0 | 20 | MG | |||||||||
| 125725011 | 12572501 | 5 | SS | NADOLOL. | NADOLOL | 1 | Unknown | 0 | 20 | MG | |||||||||
| 125725011 | 12572501 | 6 | SS | VITAMIN D3 | CHOLECALCIFEROL | 1 | Oral | 0 | 200 | IU | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125725011 | 12572501 | 1 | Hepatic cirrhosis |
| 125725011 | 12572501 | 2 | Product used for unknown indication |
| 125725011 | 12572501 | 3 | Product used for unknown indication |
| 125725011 | 12572501 | 4 | Product used for unknown indication |
| 125725011 | 12572501 | 5 | Product used for unknown indication |
| 125725011 | 12572501 | 6 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125725011 | 12572501 | Diarrhoea | |
| 125725011 | 12572501 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 125725011 | 12572501 | 1 | 2016 | 0 |