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
127733421 12773342 1 I 20160915 20160922 20160922 EXP NL-ASTRAZENECA-2016SE99606 ASTRAZENECA 0.00 M Y 0.00000 20160923 CN 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
127733421 12773342 1 PS ZOLADEX GOSERELIN ACETATE 1 Subcutaneous U 19726 10.8 MG IMPLANT
127733421 12773342 2 SS ZOLADEX GOSERELIN ACETATE 1 Subcutaneous 12.8MG UNKNOWN U 19726 12.8 MG IMPLANT

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127733421 12773342 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127733421 12773342 Fatigue
127733421 12773342 Hot flush
127733421 12773342 Overdose
127733421 12773342 Pruritus
127733421 12773342 Shock

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

no results found

Therapies reported

no results found