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
125266101 12526610 1 I 20160701 20160705 20160705 EXP PHHY2016ZA091304 NOVARTIS 89.00 YR F Y 0.00000 20160705 CN COUNTRY NOT SPECIFIED ZA

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
125266101 12526610 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous drip 5 MG/100 ML, Q12MO 21817 5 MG SOLUTION FOR INJECTION
125266101 12526610 2 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous drip 5 MG/100 ML, Q12MO 21817 5 MG SOLUTION FOR INJECTION
125266101 12526610 3 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous drip 5 MG/100 ML, Q12MO 21817 5 MG SOLUTION FOR INJECTION
125266101 12526610 4 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous drip 5 MG/100 ML, Q12MO 21817 5 MG SOLUTION FOR INJECTION
125266101 12526610 5 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous drip 5 MG/100 ML, Q12MO 21817 5 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125266101 12526610 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
125266101 12526610 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125266101 12526610 Malaise
125266101 12526610 Pneumonia

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
125266101 12526610 1 201006 0
125266101 12526610 2 2011 0
125266101 12526610 3 2012 0
125266101 12526610 4 2013 0
125266101 12526610 5 2014 2014 0