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
126498361 12649836 1 I 20160707 20160812 20160812 EXP US-ASTRAZENECA-2016SE74736 ASTRAZENECA 0.00 F Y 0.00000 20160813 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
126498361 12649836 1 PS FASLODEX FULVESTRANT 1 Intramuscular 21344 INJECTION
126498361 12649836 2 SS FASLODEX FULVESTRANT 1 Intramuscular 21344 100 MG INJECTION QD
126498361 12649836 3 SS IBRANCE PALBOCICLIB 1 Oral 5875 MG U U 0 125 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126498361 12649836 3 Breast cancer female

Outcome of event

Event ID CASEID OUTC COD
126498361 12649836 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126498361 12649836 Abdominal pain upper
126498361 12649836 Rash
126498361 12649836 Rash pruritic
126498361 12649836 Stomach mass
126498361 12649836 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
126498361 12649836 3 20160525 20160710 0