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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5688588 | 6558821 | F | 5688588-4 | 20071217 | 20080320 | 20080331 | EXP | PHHO2008CA02413 | NOVARTIS PHARMACEUTICALS CORP. | 68 | YR | M | Y | 105.5 | KG | 20080328 | MD | CANADA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5688588 | 1009725590 | SS | MYCOPHENOLATE MOFETIL | 1 | ORAL | 0.75 MG, BID | |||||
| 5688588 | 1009725591 | PS | NEORAL | 1 | ORAL | 275 MG DAILY | 050715 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5688588 | 1009725590 | HEART TRANSPLANT |
| 5688588 | 1009725591 | HEART TRANSPLANT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5688588 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5688588 | ENTEROCOCCAL INFECTION |
| 5688588 | PERICARDIAL DRAINAGE |
| 5688588 | PERICARDIAL EFFUSION |
| 5688588 | PLEURAL EFFUSION |
| 5688588 | THORACIC CAVITY DRAINAGE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5688588 | 1009725590 | 20071206 | 20080129 | 79200 | MIN |
| 5688588 | 1009725591 | 20071206 | 20080129 | 79200 | MIN |