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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542787 | 5706633 | I | 4542787-3 | 20040815 | 20041223 | 20041231 | EXP | PHRM2004FR03774 | NOVARTIS PHARMACEUTICALS CORP. | 43 | YR | F | Y | 20041231 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542787 | 1005547043 | PS | COTAREG | 2 | ORAL | 1 DF, QD | |||||
| 4542787 | 1005547044 | SS | FLUDEX | 2 | ORAL | 1 DF, QD | |||||
| 4542787 | 1005547045 | SS | LERCAN | 2 | ORAL | 1 DF, QD | |||||
| 4542787 | 1005547046 | C | DAFALGAN | 2 | |||||||
| 4542787 | 1005547047 | C | EUPHYLLINE | 2 | |||||||
| 4542787 | 1005547048 | C | EUPRESSYL | 2 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4542787 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4542787 | BLOOD ALDOSTERONE INCREASED |
| 4542787 | BLOOD CALCIUM DECREASED |
| 4542787 | BLOOD CREATININE INCREASED |
| 4542787 | BLOOD PHOSPHORUS INCREASED |
| 4542787 | BLOOD UREA INCREASED |
| 4542787 | C-REACTIVE PROTEIN INCREASED |
| 4542787 | DEHYDRATION |
| 4542787 | DIARRHOEA |
| 4542787 | MICROCYTIC ANAEMIA |
| 4542787 | PRIMARY HYPERALDOSTERONISM |
| 4542787 | RENAL FAILURE ACUTE |
| 4542787 | RENIN INCREASED |
| 4542787 | WEIGHT DECREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4542787 | 1005547043 | 20040914 | |||
| 4542787 | 1005547044 | 20040914 | |||
| 4542787 | 1005547045 | 20040914 |