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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123924582 | 12392458 | 2 | F | 20160628 | 20160523 | 20160712 | EXP | GB-MHRA-ADR 23376332 | GB-ACCORD-038604 | ACCORD | 47.00 | YR | F | Y | 0.00000 | 20160712 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123924582 | 12392458 | 1 | PS | FLUOROURACIL. | FLUOROURACIL | 1 | Unknown | 40743 | 3226 | DF | |||||||||
123924582 | 12392458 | 2 | SS | IRINOTECAN | IRINOTECAN | 1 | Intravenous (not otherwise specified) | 79068 | |||||||||||
123924582 | 12392458 | 3 | SS | ONDANSETRON | ONDANSETRON | 1 | Intravenous (not otherwise specified) | U | 206846 | 8 | MG | ||||||||
123924582 | 12392458 | 4 | SS | ATROPINE. | ATROPINE | 1 | Subcutaneous | U | 0 | 250 | UG | ||||||||
123924582 | 12392458 | 5 | SS | AVASTIN | BEVACIZUMAB | 1 | Intravenous (not otherwise specified) | U | 0 | 350 | MG | ||||||||
123924582 | 12392458 | 6 | SS | DEXAMETHASONE. | DEXAMETHASONE | 1 | Intravenous (not otherwise specified) | U | 0 | 6.6 | MG | ||||||||
123924582 | 12392458 | 7 | SS | EMEND | APREPITANT | 1 | Oral | U | 0 | 125 | MG | CAPSULE | |||||||
123924582 | 12392458 | 8 | SS | CALCIUM CARBONATE/CALCIUM LACTOGLUCONATE | CALCIUM CARBONATECALCIUM LACTATE GLUCONATE | 1 | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
123924582 | 12392458 | 1 | Product used for unknown indication |
123924582 | 12392458 | 2 | Product used for unknown indication |
123924582 | 12392458 | 3 | Product used for unknown indication |
123924582 | 12392458 | 4 | Product used for unknown indication |
123924582 | 12392458 | 5 | Product used for unknown indication |
123924582 | 12392458 | 6 | Product used for unknown indication |
123924582 | 12392458 | 7 | Product used for unknown indication |
123924582 | 12392458 | 8 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
123924582 | 12392458 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
123924582 | 12392458 | Anorectal disorder | |
123924582 | 12392458 | Blood urine present | |
123924582 | 12392458 | Diarrhoea | |
123924582 | 12392458 | Protein urine present |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |