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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7205504 | 7740415 | F | 7205504-4 | 20101201 | 20101228 | 20101231 | EXP | PHHY2010BE87555 | NOVARTIS PHARMACEUTICAL CORPORATION | 70 | YR | M | Y | 20101231 | MD | BELGIUM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7205504 | 1015449405 | PS | CERTICAN | 1 | UNK | 022334 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7205504 | 1015449405 | HEART TRANSPLANT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7205504 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 7205504 | GASTROINTESTINAL HAEMORRHAGE |
| 7205504 | GENERAL PHYSICAL HEALTH DETERIORATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |