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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4365383 | 4148104 | I | 4365383-X | 20040507 | 20040525 | EXP | RENA-11017 | GENZYME CORPORATION | 74 | YR | M | N | 20040520 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4365383 | 1004893133 | PS | RENAGEL | 1 | ORAL | 0.5 G TID PO | D | D | 21179 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4365383 | 1004893133 | HYPERPHOSPHATAEMIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4365383 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4365383 | INTESTINAL OBSTRUCTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4365383 | FGN |
| 4365383 | HP |
| 4365383 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4365383 | 1004893133 | 20040301 | 20040409 |