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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126364351 | 12636435 | 1 | I | 20160725 | 20160809 | 20160809 | EXP | US-ROCHE-1810520 | ROCHE | 0.00 | F | Y | 57.00000 | KG | 20160809 | OT | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126364351 | 12636435 | 1 | PS | TARCEVA | ERLOTINIB HYDROCHLORIDE | 1 | Unknown | U | 53728 | ||||||||||
126364351 | 12636435 | 2 | SS | AVASTIN | BEVACIZUMAB | 1 | Unknown | U | 125085 | ||||||||||
126364351 | 12636435 | 3 | SS | CARBOPLATIN. | CARBOPLATIN | 1 | Unknown | U | 0 | ||||||||||
126364351 | 12636435 | 4 | SS | TAXOL | PACLITAXEL | 1 | Unknown | U | 0 | ||||||||||
126364351 | 12636435 | 5 | SS | NIVOLUMAB | NIVOLUMAB | 1 | Unknown | U | 0 | ||||||||||
126364351 | 12636435 | 6 | C | CLARITIN (UNITED STATES) | 2 | 0 | |||||||||||||
126364351 | 12636435 | 7 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | 0 | ||||||||||||
126364351 | 12636435 | 8 | C | LOSARTAN. | LOSARTAN | 1 | 0 | ||||||||||||
126364351 | 12636435 | 9 | C | IBUPROFEN. | IBUPROFEN | 1 | 0 | ||||||||||||
126364351 | 12636435 | 10 | C | ALIMTA | PEMETREXED DISODIUM | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126364351 | 12636435 | 1 | Product used for unknown indication |
126364351 | 12636435 | 2 | Product used for unknown indication |
126364351 | 12636435 | 3 | Product used for unknown indication |
126364351 | 12636435 | 4 | Product used for unknown indication |
126364351 | 12636435 | 5 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126364351 | 12636435 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126364351 | 12636435 | Disease progression |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |