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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6818804 | 7469226 | I | 6818804-4 | 20100413 | 20100625 | 20100630 | EXP | 2010US002518 | ASTELLAS PHARMA GLOBAL DEVELOPMENT, INC. | 58 | YR | M | N | 20100629 | CN | 20100413 | COLOMBIA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6818804 | 1014042633 | PS | PROGRAF | 1 | 8 MG, /D | D | D | 50708 | |||
| 6818804 | 1014105621 | C | PREDNISOLONE | 1 | |||||||
| 6818804 | 1014105622 | C | MYCOPHENOLATE MOFETIL | 1 | |||||||
| 6818804 | 1014105623 | C | TRIMETOPRIM (TRIMETHOPRIM) | 2 | |||||||
| 6818804 | 1014105624 | C | NIFEDIPINE | 1 | |||||||
| 6818804 | 1014105625 | C | OMEPRAZOLE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6818804 | 1014042633 | RENAL TRANSPLANT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6818804 | DE |
| 6818804 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6818804 | CORONARY ARTERY EMBOLISM |
| 6818804 | THROMBOSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6818804 | CSM |
| 6818804 | FGN |
| 6818804 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6818804 | 1014042633 | 20090129 |