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
125970812 12597081 2 F 201601 20160725 20160727 20160729 EXP PHHY2016MX102432 NOVARTIS 40.13 YR F Y 0.00000 20160729 CN COUNTRY NOT SPECIFIED MX

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
125970812 12597081 1 PS FEMARA LETROZOLE 1 Oral 2.5 MG, QD 20726 2.5 MG TABLET QD
125970812 12597081 2 SS AFINITOR EVEROLIMUS 1 Oral 1 DF, QD 0 1 DF TABLET QD
125970812 12597081 3 C VITAMIN K PHYTONADIONE 1 Intramuscular 1 DF, Q72H 0 1 DF AMPOULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125970812 12597081 1 Breast cancer
125970812 12597081 2 Breast cancer
125970812 12597081 3 Contusion

Outcome of event

Event ID CASEID OUTC COD
125970812 12597081 OT
125970812 12597081 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125970812 12597081 Abscess jaw
125970812 12597081 Breast cancer
125970812 12597081 Haematoma
125970812 12597081 Liver injury
125970812 12597081 Metastases to bone marrow
125970812 12597081 Metastases to central nervous system
125970812 12597081 Platelet count decreased
125970812 12597081 Pleural effusion
125970812 12597081 Septic shock
125970812 12597081 Skeletal injury

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
125970812 12597081 1 20160623 0
125970812 12597081 2 2015 0
125970812 12597081 3 20160702 0