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
126552021 12655202 1 I 20160701 20160728 20160816 20160816 EXP IT-ASTRAZENECA-2016SE82641 ASTRAZENECA 63.00 YR F Y 0.00000 20160816 IT IT

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
126552021 12655202 1 PS FASLODEX FULVESTRANT 1 Intramuscular U U 0 INJECTION
126552021 12655202 2 SS PALBOCICLIB PALBOCICLIB 1 Oral 1875 MG Y U 0 125 MG CAPSULE QD
126552021 12655202 3 C NEBILOX NEBIVOLOL HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126552021 12655202 1 Breast cancer
126552021 12655202 2 Breast cancer
126552021 12655202 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126552021 12655202 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126552021 12655202 Neutropenia
126552021 12655202 Off label use

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
126552021 12655202 1 20160422 0
126552021 12655202 2 20160617 0