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
107772075 10777207 5 F 20131126 20160921 20150209 20160926 EXP PHHY2015VE015334 NOVARTIS 70.28 YR F Y 0.00000 20160926 MD VE VE

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
107772075 10777207 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, Q12MO (ANNUALLY) D 21817 5 MG SOLUTION FOR INJECTION
107772075 10777207 2 SS ACLASTA ZOLEDRONIC ACID 1 Subcutaneous 5 MG, Q12MO (ANNUALLY) D 21817 5 MG SOLUTION FOR INJECTION
107772075 10777207 3 SS ACLASTA ZOLEDRONIC ACID 1 Unknown 5 MG, Q12MO (ANNUALLY) D 21817 5 MG SOLUTION FOR INJECTION
107772075 10777207 4 SS ACLASTA ZOLEDRONIC ACID 1 Unknown 5 MG, Q12MO D 21817 5 MG SOLUTION FOR INJECTION
107772075 10777207 5 C BONAMES 2 Oral 1 DF, QMO U 0 1 DF /month
107772075 10777207 6 C CALCIUM CALCIUM 1 Oral 1 DF, QD U 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107772075 10777207 1 Osteoporosis
107772075 10777207 5 Osteopenia
107772075 10777207 6 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
107772075 10777207 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
107772075 10777207 Accident
107772075 10777207 Fall
107772075 10777207 Femur fracture
107772075 10777207 Hand fracture
107772075 10777207 Incorrect route of drug administration

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
107772075 10777207 1 20120323 0
107772075 10777207 2 20131126 0
107772075 10777207 3 2014 0