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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5795550 | 6663753 | F | 5795550-X | 20071231 | 20080619 | 20080630 | EXP | PHHO2008DE07199 | NOVARTIS PHARMACEUTICALS CORP. | M | Y | 86 | KG | 20080627 | MD | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5795550 | 1010112643 | PS | ERL 080A ERL+TAB | 2 | ORAL | 2160 MG, DAILY | 50791 | ||||
| 5795550 | 1010112644 | SS | ERL 080A ERL+TAB | 2 | ORAL | 1440 MG, DAILY | 050791 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5795550 | 1010112643 | RENAL TRANSPLANT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5795550 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5795550 | BLOOD CREATININE INCREASED |
| 5795550 | DEHYDRATION |
| 5795550 | DIARRHOEA |
| 5795550 | RENAL FAILURE ACUTE |
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 |
|---|---|---|---|---|---|
| 5795550 | 1010112643 | 20071206 | 20080101 | 27 | DAY |
| 5795550 | 1010112644 | 20080102 |