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
126075671 12607567 1 I 20160619 20160727 20160729 20160729 EXP PHHY2016CA104116 NOVARTIS 93.68 YR M Y 0.00000 20160729 CN COUNTRY NOT SPECIFIED CA

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
126075671 12607567 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK 21817 5 MG SOLUTION FOR INJECTION
126075671 12607567 2 SS ACLASTA ZOLEDRONIC ACID 1 Unknown 21817 SOLUTION FOR INJECTION
126075671 12607567 3 SS ACLASTA ZOLEDRONIC ACID 1 Unknown 21817 SOLUTION FOR INJECTION
126075671 12607567 4 SS ACLASTA ZOLEDRONIC ACID 1 Unknown 21817 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126075671 12607567 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
126075671 12607567 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126075671 12607567 Death

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
126075671 12607567 1 20120627 0
126075671 12607567 2 20130819 0
126075671 12607567 3 20140902 0
126075671 12607567 4 20150904 20150904 0