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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5327083 | 6314190 | I | 5327083-9 | 20070507 | 20070517 | EXP | PHEH2007US07178 | NOVARTIS PHARMACEUTICALS CORP. | 71 | YR | M | Y | 20070517 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5327083 | 1008487299 | PS | SANDIMMUNE | 1 | ORAL | 75 MG AM AND 50 MG PM PER DAY | 50625 | ||||
| 5327083 | 1008487300 | SS | CYCLOSPORINE | 1 | ORAL | 75 MG AM AND 50 MG PM |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5327083 | 1008487299 | HEART TRANSPLANT |
| 5327083 | 1008487300 | HEART TRANSPLANT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5327083 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5327083 | CATARACT |
| 5327083 | DEAFNESS |
| 5327083 | HYPOAESTHESIA |
| 5327083 | NEUROPATHY PERIPHERAL |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |