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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125686411 | 12568641 | 1 | I | 20160715 | 20160719 | 20160719 | EXP | GB-ROCHE-1795725 | ROCHE | 57.00 | YR | M | Y | 0.00000 | 20160719 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125686411 | 12568641 | 1 | PS | AVASTIN | BEVACIZUMAB | 1 | Unknown | U | U | 125085 | SOLUTION FOR INFUSION | ||||||||
125686411 | 12568641 | 2 | SS | APREPITANT. | APREPITANT | 1 | Unknown | U | U | 0 | |||||||||
125686411 | 12568641 | 3 | SS | ATROPINE. | ATROPINE | 1 | Unknown | U | U | 0 | |||||||||
125686411 | 12568641 | 4 | SS | DEXAMETHASONE. | DEXAMETHASONE | 1 | Unknown | U | U | 0 | |||||||||
125686411 | 12568641 | 5 | SS | IRINOTECAN | IRINOTECAN | 1 | Unknown | U | U | 0 | |||||||||
125686411 | 12568641 | 6 | SS | ONDANSETRON | ONDANSETRON | 1 | Unknown | U | U | 0 | |||||||||
125686411 | 12568641 | 7 | SS | TRAMADOL HYDROCHLORIDE. | TRAMADOL HYDROCHLORIDE | 1 | Unknown | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125686411 | 12568641 | 1 | Product used for unknown indication |
125686411 | 12568641 | 2 | Product used for unknown indication |
125686411 | 12568641 | 3 | Product used for unknown indication |
125686411 | 12568641 | 4 | Product used for unknown indication |
125686411 | 12568641 | 5 | Product used for unknown indication |
125686411 | 12568641 | 6 | Product used for unknown indication |
125686411 | 12568641 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125686411 | 12568641 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125686411 | 12568641 | Decreased appetite | |
125686411 | 12568641 | Emotional disorder | |
125686411 | 12568641 | Fatigue | |
125686411 | 12568641 | Gait disturbance | |
125686411 | 12568641 | Hypertension | |
125686411 | 12568641 | Ill-defined disorder | |
125686411 | 12568641 | Mouth ulceration |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |