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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6738844 | 7399734 | I | 6738844-3 | 20090713 | 20100514 | 20100520 | EXP | 2009SP028257 | SCHERING-PLOUGH CORPORATION | 44 | YR | M | N | 20100519 | JAPAN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6738844 | 1013742319 | PS | TEMODAL | 1 | ORAL | 150 MG/M2; PO | D | D | 21029 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6738844 | 1013742319 | ANAPLASTIC ASTROCYTOMA |
Outcome of event
Event ID | OUTC COD |
---|---|
6738844 | OT |
Reactions reported
Event ID | PT |
---|---|
6738844 | APHASIA |
6738844 | HEMIPLEGIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6738844 | CR |
6738844 | FGN |
6738844 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6738844 | 1013742319 | 20090706 |