Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6527765 | 7247099 | I | 6527765-7 | 20070301 | 20091221 | 20091231 | EXP | 003557 | UCB, INC. | 66 | YR | M | N | 20091230 | DENMARK |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6527765 | 1012903996 | PS | METOLAZONE | 1 | (2.5 MG QD) | Y | 17386 | ||||
| 6527765 | 1012950608 | SS | FUROSEMIDE | 1 | (40 MG TID), (), (DOSE INCREASED) | Y | N | ||||
| 6527765 | 1012950614 | SS | SPIRONOLACTONE | 1 | (12.5 MG QD) | D | D | ||||
| 6527765 | 1012950616 | SS | RAMIPRIL | 1 | (7.5 MG, 5MG IN THE MORNING AND 2.5 MG AT NIGHT), (DOSAGE ADJUSTED) | D |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6527765 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6527765 | AZOTAEMIA |
| 6527765 | BLOOD SODIUM DECREASED |
| 6527765 | DEHYDRATION |
| 6527765 | FATIGUE |
| 6527765 | HYPOTENSION |
| 6527765 | RENAL DISORDER |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6527765 | FGN |
| 6527765 | HP |
| 6527765 | LIT |
| 6527765 | OTH |
Therapies reported
| no results found |