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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4327765 | 3966140 | F | 4327765-1 | 20020101 | 20030613 | 20040331 | EXP | PHBS2003JP06217 | NOVARTIS PHARMACEUTICALS CORP. | 64 | YR | F | Y | 20040331 | MD | 20030501 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4327765 | 1004748391 | PS | GLEEVEC | 1 | ORAL | UNK, Q48H | |||||
| 4327765 | 1004748392 | SS | GLEEVEC | 1 | ORAL | 200 MG, BID |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4327765 | 1004748391 | GASTROINTESTINAL CARCINOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4327765 | DE |
| 4327765 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4327765 | ABDOMINAL PAIN |
| 4327765 | ABDOMINAL PAIN UPPER |
| 4327765 | DIARRHOEA |
| 4327765 | LIVER CARCINOMA RUPTURED |
| 4327765 | METASTASES TO PERITONEUM |
| 4327765 | PERITONITIS |
| 4327765 | RASH |
| 4327765 | THROMBOCYTOPENIA |
| 4327765 | TUMOUR HAEMORRHAGE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4327765 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4327765 | 1004748391 | 20020101 | |||
| 4327765 | 1004748392 | 20020301 | 20020101 |