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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
117195772 | 11719577 | 2 | F | 20151029 | 20160907 | 20151110 | 20160916 | EXP | US-PFIZER INC-2015372298 | PFIZER | 40.00 | YR | F | Y | 83.00000 | KG | 20160916 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
117195772 | 11719577 | 1 | PS | CRIZOTINIB | CRIZOTINIB | 1 | Oral | 250 MG, ONCE DAILY | 4000 | MG | N | 202570 | 250 | MG | TABLET | QD | |||
117195772 | 11719577 | 2 | SS | ITRACONAZOLE. | ITRACONAZOLE | 1 | Oral | 200 MG, ONCE DAILY | 3200 | MG | N | 0 | 200 | MG | CAPSULE | QD | |||
117195772 | 11719577 | 3 | C | NORCO | ACETAMINOPHENHYDROCODONE BITARTRATE | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
117195772 | 11719577 | 1 | Cervix carcinoma |
117195772 | 11719577 | 3 | Pain |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
117195772 | 11719577 | OT |
117195772 | 11719577 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
117195772 | 11719577 | Thrombocytopenia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
117195772 | 11719577 | 1 | 20151006 | 20151021 | 0 | |
117195772 | 11719577 | 2 | 20151006 | 20151021 | 0 |