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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5851028 | 6743787 | I | 5851028-6 | 20080709 | 20080818 | EXP | RENA-1000210 | GENZYME | N | 20080815 | MD | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5851028 | 1010328741 | PS | RENAGEL | 1 | ORAL | ORAL | U | U | 21179 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5851028 | 1010328741 | HYPERPHOSPHATAEMIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5851028 | DS |
Reactions reported
| Event ID | PT |
|---|---|
| 5851028 | DIVERTICULITIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5851028 | FGN |
| 5851028 | HP |
| 5851028 | OTH |
Therapies reported
| no results found |