Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123834182 | 12383418 | 2 | F | 20160711 | 20160518 | 20160721 | EXP | GB-TEVA-640717ACC | TEVA | 47.00 | YR | F | Y | 0.00000 | 20160721 | OT | GB | GB |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123834182 | 12383418 | 1 | PS | IRINOTECAN | IRINOTECAN | 1 | Intravenous (not otherwise specified) | U | 78122 | ||||||||||
| 123834182 | 12383418 | 2 | SS | ONDANSETRON | ONDANSETRON | 1 | Intravenous (not otherwise specified) | U | U | 76759 | 8 | MG | |||||||
| 123834182 | 12383418 | 3 | SS | 5-FLUOROURACIL | FLUOROURACIL | 1 | Unknown | 3226 (UNITS UNSPECIFIED) | U | 0 | |||||||||
| 123834182 | 12383418 | 4 | SS | ATROPINE. | ATROPINE | 1 | Subcutaneous | U | U | 0 | 250 | UG | |||||||
| 123834182 | 12383418 | 5 | SS | AVASTIN | BEVACIZUMAB | 1 | Intravenous (not otherwise specified) | U | U | 0 | 350 | MG | |||||||
| 123834182 | 12383418 | 6 | SS | DEXAMETHASON | DEXAMETHASONE | 1 | Intravenous (not otherwise specified) | U | U | 0 | 6.6 | MG | INJECTION | ||||||
| 123834182 | 12383418 | 7 | SS | EMEND | APREPITANT | 1 | Oral | U | U | 0 | 125 | MG | CAPSULE | ||||||
| 123834182 | 12383418 | 8 | SS | CALCIUM | CALCIUM | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123834182 | 12383418 | 1 | Product used for unknown indication |
| 123834182 | 12383418 | 2 | Product used for unknown indication |
| 123834182 | 12383418 | 3 | Product used for unknown indication |
| 123834182 | 12383418 | 4 | Product used for unknown indication |
| 123834182 | 12383418 | 5 | Product used for unknown indication |
| 123834182 | 12383418 | 6 | Product used for unknown indication |
| 123834182 | 12383418 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123834182 | 12383418 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123834182 | 12383418 | Anorectal disorder | |
| 123834182 | 12383418 | Diarrhoea |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |