The Safety Rates Drug Report

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Drug     Injury     Quarter    

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