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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8248766 | 8469810 | F | 8248766-7 | 20120217 | 20120328 | 20120331 | EXP | PHHY2012AU022852 | NOVARTIS PHARMACEUTICAL CORPORATION | 44 | YR | F | Y | 20120330 | MD | AUSTRALIA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8248766 | 1019282809 | C | VESICARE | 1 | |||||||
8248766 | 1019282808 | PS | GILENYA | 1 | ORAL | 0.5 MG, QD | 022527 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
8248766 | OT |
Reactions reported
Event ID | PT |
---|---|
8248766 | SKIN DISCOLOURATION |
8248766 | MALIGNANT MELANOMA |
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 |
---|---|---|---|---|---|
8248766 | 1019282809 | 20110101 | |||
8248766 | 1019282808 | 20111113 | 20120301 | 110 | DAY |