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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5483695 | 6444544 | I | 5483695-3 | 20070820 | 20070924 | 20071010 | EXP | WAES 0709USA04109 | MERCK + CO., INC. | 64 | YR | M | N | 189 | LBS | 20071005 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5483695 | 1009033529 | SS | DECADRON | 1 | U | D | 11664 | ||||
| 5483695 | 1009054218 | PS | ARANESP | 1 | SUBCUTANEOUS | 500 MICROGM/SC INJ | D | D | |||
| 5483695 | 1009054241 | SS | GRANISETRON HCL | 1 | U | D | |||||
| 5483695 | 1009054243 | SS | OXALIPLATIN | 1 | U | D | |||||
| 5483695 | 1009054244 | SS | CAPECITABINE | 2 | U | D | |||||
| 5483695 | 1009054246 | C | ZIAC | 1 | |||||||
| 5483695 | 1009054247 | C | ASPIRIN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5483695 | 1009054218 | ANAEMIA |
| 5483695 | 1009054218 | POST PROCEDURAL COMPLICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5483695 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5483695 | ASTHENIA |
| 5483695 | CONDITION AGGRAVATED |
| 5483695 | DEHYDRATION |
| 5483695 | DIARRHOEA |
| 5483695 | ENTEROCOLITIS |
| 5483695 | POST PROCEDURAL COMPLICATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5483695 | HP |
| 5483695 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5483695 | 1009054218 | 20070813 | 20070813 | ||
| 5483695 | 1009054244 | 20070820 |