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
113415484 11341548 4 F 201506 20160706 20150805 20160712 EXP PHHY2015ZA091555 NOVARTIS 70.33 YR F Y 0.00000 20160712 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
113415484 11341548 1 PS ACLASTA ZOLEDRONIC ACID 1 Unknown 1 DF, Q12MO 21817 1 DF SOLUTION FOR INJECTION
113415484 11341548 2 SS ACLASTA ZOLEDRONIC ACID 1 Unknown 1 DF, Q12MO 21817 1 DF SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113415484 11341548 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
113415484 11341548 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113415484 11341548 Contusion
113415484 11341548 Facial bones fracture
113415484 11341548 Facial pain
113415484 11341548 Fall
113415484 11341548 Haematoma
113415484 11341548 Limb injury

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
113415484 11341548 1 201404 0
113415484 11341548 2 2015 0