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
125278771 12527877 1 I 20160627 20160705 20160705 EXP GB-ASTRAZENECA-2016SE70357 ASTRAZENECA 39.00 YR F Y 0.00000 20160705 MD GB GB

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
125278771 12527877 1 PS ZOLADEX GOSERELIN ACETATE 1 Subcutaneous U U 19726 IMPLANT
125278771 12527877 2 SS AFINITOR EVEROLIMUS 1 Unknown U U 0
125278771 12527877 3 SS EXEMESTANE. EXEMESTANE 1 Unknown U U 0
125278771 12527877 4 SS ZOMETA ZOLEDRONIC ACID 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125278771 12527877 1 Breast cancer
125278771 12527877 2 Breast cancer
125278771 12527877 3 Breast cancer
125278771 12527877 4 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
125278771 12527877 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125278771 12527877 Malignant neoplasm progression
125278771 12527877 Mucosal inflammation
125278771 12527877 Palmar-plantar erythrodysaesthesia syndrome

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found