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
123151212 12315121 2 F 201603 20160629 20160428 20160707 PER US-ASTRAZENECA-2016SE42991 ASTRAZENECA 895.00 MON F Y 73.00000 KG 20160707 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
123151212 12315121 1 PS ANASTROZOLE. ANASTROZOLE 1 Oral U 20541 TABLET
123151212 12315121 2 SS AROMASIN EXEMESTANE 1 Unknown Y 0 45 MG TABLET QD
123151212 12315121 3 SS LETROZOLE. LETROZOLE 1 Unknown U 0
123151212 12315121 4 C EDARBI AZILSARTAN KAMEDOXOMIL 1 0 40 MG QD
123151212 12315121 5 C AMLODIPINE AMLODIPINE BESYLATE 1 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123151212 12315121 4 Blood pressure abnormal
123151212 12315121 5 Blood pressure abnormal

Outcome of event

Event ID CASEID OUTC COD
123151212 12315121 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123151212 12315121 Alopecia
123151212 12315121 Arthritis
123151212 12315121 Back disorder
123151212 12315121 Confusional state
123151212 12315121 Depressed mood
123151212 12315121 Disease recurrence
123151212 12315121 Gait disturbance
123151212 12315121 Joint swelling
123151212 12315121 Malaise
123151212 12315121 Memory impairment
123151212 12315121 Morbid thoughts
123151212 12315121 Peripheral swelling
123151212 12315121 Visual acuity reduced
123151212 12315121 Weight increased

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
123151212 12315121 2 20160301 201603 0