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
127871401 12787140 1 I 20160420 20160628 20160927 20160927 EXP NL-ASTRAZENECA-2016SE71117 ASTRAZENECA 25758.00 DY M Y 0.00000 20160928 OT NL NL

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
127871401 12787140 1 PS ZOLADEX GOSERELIN ACETATE 1 Subcutaneous 10.8 MG U LV871 20578 IMPLANT
127871401 12787140 2 SS ZOLADEX GOSERELIN ACETATE 1 Subcutaneous 10.8 MG U LY223 20578 IMPLANT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127871401 12787140 1 Prostate cancer
127871401 12787140 2 Prostate cancer

Outcome of event

Event ID CASEID OUTC COD
127871401 12787140 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127871401 12787140 Cardiac arrest
127871401 12787140 Hot flush

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
127871401 12787140 1 20160405 0
127871401 12787140 2 20160627 0