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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127815281 | 12781528 | 1 | I | 20150420 | 20160919 | 20160926 | 20160926 | EXP | ES-AGEMED-742755340 | ES-PFIZER INC-2016440899 | PFIZER | 52.00 | YR | F | Y | 0.00000 | 20160926 | MD | ES | ES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127815281 | 12781528 | 1 | PS | ALDACTONE | SPIRONOLACTONE | 1 | Oral | Y | 12151 | FILM-COATED TABLET | |||||||||
| 127815281 | 12781528 | 2 | I | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | Y | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127815281 | 12781528 | 1 | Hepatic cirrhosis |
| 127815281 | 12781528 | 2 | Hepatic cirrhosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127815281 | 12781528 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127815281 | 12781528 | Drug interaction | |
| 127815281 | 12781528 | Hepatic encephalopathy |
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 |
|---|---|---|---|---|---|---|
| 127815281 | 12781528 | 1 | 20150414 | 20150426 | 0 | |
| 127815281 | 12781528 | 2 | 20150414 | 20150426 | 0 |