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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6195505 | 6998075 | I | 6195505-X | 20090317 | 20090506 | 20090519 | EXP | PHHY2009ES16994 | NOVARTIS PHARMACEUTICALS CORP. | 42 | YR | M | Y | 20090519 | MD | SPAIN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6195505 | 1011595086 | PS | GLEEVEC | 1 | ORAL | 400 MG/DAY | 021588 | ||||
6195505 | 1011595087 | SS | GLEEVEC | 1 | 300 MG, UNK | 021588 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6195505 | 1011595086 | CHRONIC MYELOID LEUKAEMIA |
Outcome of event
Event ID | OUTC COD |
---|---|
6195505 | OT |
Reactions reported
Event ID | PT |
---|---|
6195505 | FOOD POISONING |
6195505 | SKIN LESION |
6195505 | THROMBOCYTOPENIA |
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 |
---|---|---|---|---|---|
6195505 | 1011595086 | 20081003 | 20090317 | 166 | DAY |