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
118729675 11872967 5 F 20151222 20160915 20151228 20160927 PER US-PFIZER INC-2015462956 PFIZER 73.00 YR F Y 89.00000 KG 20160927 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
118729675 11872967 1 PS IBRANCE PALBOCICLIB 1 Oral 125 MG, CYCLIC (DAY 1-21 Q 28 DAYS) Y M29120 207103 125 MG CAPSULE
118729675 11872967 2 SS IBRANCE PALBOCICLIB 1 Oral 100 MG, DAY 1-21 Q28 D Y M24336 207103 100 MG CAPSULE
118729675 11872967 3 SS IBRANCE PALBOCICLIB 1 Oral 75 MG, CYCLIC (DAYS 1-21 Q28 DAYS) Y M86440 207103 75 MG CAPSULE
118729675 11872967 4 SS IBRANCE PALBOCICLIB 1 Oral 75 MG, CYCLIC (1D-21 D Q 28D) Y R10405 207103 75 MG CAPSULE
118729675 11872967 5 SS NEUPOGEN FILGRASTIM 1 UNK U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118729675 11872967 1 Breast cancer metastatic
118729675 11872967 2 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
118729675 11872967 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118729675 11872967 Fatigue
118729675 11872967 Nausea
118729675 11872967 Neutropenia
118729675 11872967 White blood cell count decreased

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
118729675 11872967 1 20151207 0
118729675 11872967 3 20151207 20160520 0
118729675 11872967 4 20151207 0
118729675 11872967 5 201409 0