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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5904417 | 6781913 | I | 5904417-5 | 20080927 | 20080930 | DIR | 30 | YR | M | N | 158 | LBS | 20080929 | PH | N | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5904417 | 1010523901 | PS | GLEEVEC | 1 | ORAL | 400 MG DAILY PO | Y | D |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5904417 | 1010523901 | CHRONIC MYELOID LEUKAEMIA |
Outcome of event
Event ID | OUTC COD |
---|---|
5904417 | HO |
Reactions reported
Event ID | PT |
---|---|
5904417 | ABASIA |
5904417 | MUSCLE HAEMORRHAGE |
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 |
---|---|---|---|---|---|
5904417 | 1010523901 | 20080917 | 20080926 |