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
127268401 12726840 1 I 201603 20160615 20160908 20160908 PER US-ASTRAZENECA-2016SE66461 ASTRAZENECA 0.00 F Y 0.00000 20160909 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
127268401 12726840 1 PS ANASTRAZOLE ANASTROZOLE 1 Oral U 20541 TABLET
127268401 12726840 2 SS AROMASIN EXEMESTANE 1 Oral ONCE DAILY AFTER MEAL U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127268401 12726840 1 Breast cancer female

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127268401 12726840 Abdominal discomfort
127268401 12726840 Depression
127268401 12726840 Flushing
127268401 12726840 Grip strength decreased
127268401 12726840 Headache
127268401 12726840 Hyperhidrosis
127268401 12726840 Insomnia
127268401 12726840 Limb discomfort
127268401 12726840 Myalgia
127268401 12726840 Pain
127268401 12726840 Pain in extremity

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
127268401 12726840 1 201603 0