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
126485643 12648564 3 F 20160922 20160812 20160930 EXP CN-ASTRAZENECA-2016SE85178 ASTRAZENECA 67.00 YR M Y 0.00000 20160930 CN CN CN

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
126485643 12648564 1 PS ZOLADEX GOSERELIN ACETATE 1 Subcutaneous U 19726 3.6 MG IMPLANT
126485643 12648564 2 SS ZOLADEX GOSERELIN ACETATE 1 Subcutaneous U 19726 3.6 MG IMPLANT
126485643 12648564 3 SS CASODEX BICALUTAMIDE 1 Oral DAILY 0 TABLET
126485643 12648564 4 C CEREBROLYSIN CEREBROLYSIN 1 0
126485643 12648564 5 C ASPIRIN. ASPIRIN 1 ENTERIC-COATED TABLETS ONE TABLET DAILY 0
126485643 12648564 6 C INDAPAMIDE. INDAPAMIDE 1 0 1 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126485643 12648564 1 Prostate cancer
126485643 12648564 2 Prostate cancer
126485643 12648564 4 Cerebral infarction
126485643 12648564 5 Hypertension
126485643 12648564 6 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126485643 12648564 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126485643 12648564 Malignant neoplasm progression

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
126485643 12648564 1 20160210 0
126485643 12648564 2 20160831 0
126485643 12648564 3 20160205 0