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
119107592 11910759 2 F 20160902 20160112 20160914 EXP US-PFIZER INC-2015477964 PFIZER 59.00 YR F Y 0.00000 20160914 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
119107592 11910759 1 PS IBRANCE PALBOCICLIB 1 125 MG, CYCLIC (21 DAYS THEN 7 DAYS) U 207103 125 MG CAPSULE
119107592 11910759 2 SS FEMARA LETROZOLE 1 UNK U 0
119107592 11910759 3 C VICODIN ACETAMINOPHENHYDROCODONE BITARTRATE 1 UNK DF, AS NEEDED (5/300, 1 Q 4-6 HOURS P.R.N) 0
119107592 11910759 4 C XGEVA DENOSUMAB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119107592 11910759 1 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
119107592 11910759 DS
119107592 11910759 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119107592 11910759 Back pain
119107592 11910759 Bone marrow failure
119107592 11910759 Musculoskeletal chest pain
119107592 11910759 Pain in extremity
119107592 11910759 Urinary tract infection

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found