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
105746564 10574656 4 F 20160711 20141110 20160715 PER US-PFIZER INC-2014304960 PFIZER 83.00 YR F Y 0.00000 20160715 CN 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
105746564 10574656 1 PS AROMASIN EXEMESTANE 1 Oral 25 MG, DAILY (1 PILL DAILY AFTER MEALS) X270F 20753 25 MG COATED TABLET
105746564 10574656 2 SS AROMASIN EXEMESTANE 1 20753 COATED TABLET
105746564 10574656 3 SS AROMASIN EXEMESTANE 1 20753 COATED TABLET
105746564 10574656 4 SS AROMASIN EXEMESTANE 1 20753 COATED TABLET
105746564 10574656 5 C XGEVA DENOSUMAB 1 120 MG, UNK 0 120 MG
105746564 10574656 6 C CALCIUM WITH D CALCIUMVITAMIN D 1 600 IU, UNK 0 600 IU
105746564 10574656 7 C WARFARIN WARFARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105746564 10574656 1 Breast cancer
105746564 10574656 2 Bone cancer
105746564 10574656 3 Recurrent cancer
105746564 10574656 4 Breast cancer female
105746564 10574656 5 Recurrent cancer

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
105746564 10574656 Dizziness
105746564 10574656 Fatigue
105746564 10574656 Headache

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
105746564 10574656 1 201408 0
105746564 10574656 5 201408 0
105746564 10574656 6 201408 0