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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8478162 | 8566383 | F | 8478162-9 | 20120512 | 20120626 | 20120629 | EXP | PHEH2012US010109 | NOVARTIS PHARMACEUTICAL CORPORATION | 59 | YR | F | Y | 20120629 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
8478162 | 1020126079 | PS | GILENYA | 1 | ORAL | 0.5 MG, QD | 022527 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
8478162 | 1020126079 | MULTIPLE SCLEROSIS |
Outcome of event
Event ID | OUTC COD |
---|---|
8478162 | HO |
Reactions reported
Event ID | PT |
---|---|
8478162 | ABDOMINAL PAIN |
8478162 | VOMITING |
8478162 | DIARRHOEA |
8478162 | COLITIS |
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 |
---|---|---|---|---|---|
8478162 | 1020126079 | 20120208 |