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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5040500 | 6075485 | F | 5040500-7 | 20060402 | 20060410 | 20060630 | EXP | AU-ROCHE-443861 | ROCHE | 51 | YR | M | Y | 55 | KG | 20060630 | MD | AUSTRALIA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5040500 | 1007431426 | PS | CAPECITABINE | 2 | ORAL | GIVEN FROM DAYS ONE TO FOURTEEN OF A THREE WEEK CYCLE. | C209973 | 20896 | |||
5040500 | 1007431427 | SS | CAPECITABINE | 2 | ORAL | ON DAYS ONE TO FOURTEEN EVERY THREE WEEKS | C209973 | 020896 | |||
5040500 | 1007431428 | SS | CISPLATIN | 1 | INTRAVENOUS | GIVEN ON DAYS ONE OF A THREE WEEK CYCLE. | 500650 | ||||
5040500 | 1007431429 | C | ENDONE | 2 | AS NEEDED | ||||||
5040500 | 1007431430 | C | PANTOPRAZOLE | 2 | |||||||
5040500 | 1007431431 | C | NILSTAT | 1 | |||||||
5040500 | 1007431432 | C | TEMAZEPAM | 1 | AS NEEDED | ||||||
5040500 | 1007431433 | C | FISH OIL | 2 | |||||||
5040500 | 1007431434 | C | MAXOLON | 1 | AS NEEDED | ||||||
5040500 | 1007431435 | C | NAVOBAN | 2 | |||||||
5040500 | 1007431436 | C | ATIVAN | 1 | |||||||
5040500 | 1007431437 | C | COLOXYL WITH SENNA | 2 | |||||||
5040500 | 1007431438 | C | DEXAMETHASONE TAB | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5040500 | 1007431426 | GASTRIC CANCER |
5040500 | 1007431428 | GASTRIC CANCER |
Outcome of event
Event ID | OUTC COD |
---|---|
5040500 | HO |
5040500 | LT |
Reactions reported
Event ID | PT |
---|---|
5040500 | ANOREXIA |
5040500 | ASTHENIA |
5040500 | ENCEPHALITIS |
5040500 | GRAND MAL CONVULSION |
5040500 | NAUSEA |
5040500 | RENAL FAILURE ACUTE |
5040500 | VOMITING |
5040500 | WEIGHT DECREASED |
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 |
---|---|---|---|---|---|
5040500 | 1007431426 | 20060330 | 20060408 | 10 | DAY |
5040500 | 1007431427 | 20060409 | 20060517 | 39 | DAY |
5040500 | 1007431428 | 20060330 | 20060511 | 43 | DAY |
5040500 | 1007431429 | 20060224 | 20060516 | 82 | DAY |
5040500 | 1007431434 | 20060430 | 20060516 | 17 | DAY |
5040500 | 1007431435 | 20060508 | 20060516 | 9 | DAY |
5040500 | 1007431436 | 20060508 | 20060516 | 9 | DAY |
5040500 | 1007431437 | 20060330 | 20060516 | 48 | DAY |
5040500 | 1007431438 | 20060508 | 20060516 | 9 | DAY |