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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5847691 | 6729165 | I | 5847691-6 | 20080701 | 20080806 | 20080818 | EXP | US-AMGEN-US300275 | AMGENSAFETY | M | Y | 20080818 | CN | 20080729 | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5847691 | 1010316761 | PS | PROCRIT | 1 | SUBCUTANEOUS | UNKNOWN | |||||
| 5847691 | 1010316762 | C | LASIX | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5847691 | 1010316761 | MYELODYSPLASTIC SYNDROME |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5847691 | DE |
| 5847691 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5847691 | CARDIAC FAILURE CONGESTIVE |
| 5847691 | HEPATIC FAILURE |
| 5847691 | RENAL FAILURE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |