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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5630402 | 6555896 | I | 5630402-7 | 20060207 | 20080208 | 20080219 | EXP | PHEH2008US01756 | NOVARTIS PHARMACEUTICALS CORP. | F | Y | 20080218 | LW | 20060720 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5630402 | 1009532796 | PS | ELIDEL | 1 | TOPICAL | UNK, UNK | 021302 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5630402 | 1009532796 | ECZEMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5630402 | DE |
| 5630402 | HO |
| 5630402 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5630402 | ACUTE LEUKAEMIA |
| 5630402 | ACUTE MYELOID LEUKAEMIA |
| 5630402 | CONTUSION |
| 5630402 | PALLOR |
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 |
|---|---|---|---|---|---|
| 5630402 | 1009532796 | 20021206 | 20051212 | 1103 | DAY |