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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5120028 | 6144971 | I | 5120028-6 | 20040325 | 20060914 | 20060929 | EXP | 2006EU002569 | ASTELLAS PHARMA US, INC. | 23 | YR | F | N | 20060921 | MD | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5120028 | 1007726840 | PS | PROGRAF | 1 | ORAL | D, ORAL; ORAL | U | U | 50708 | ||
| 5120028 | 1007747161 | C | IMUREL | 2 | |||||||
| 5120028 | 1007747163 | C | SOLUPRED (PREDNISOLONE SODIUM SULFOBENZOATE) | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5120028 | 1007726840 | HEART TRANSPLANT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5120028 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5120028 | CORONARY ARTERY DISEASE |
| 5120028 | DRUG EXPOSURE BEFORE PREGNANCY |
| 5120028 | PREGNANCY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5120028 | FGN |
| 5120028 | HP |
| 5120028 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5120028 | 1007726840 | 20010205 | 20030303 | ||
| 5120028 | 1007726840 | 20040301 |