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
116528915 11652891 5 F 20150619 20160829 20151022 20160831 EXP PHHY2012CA020392 NOVARTIS 78.94 YR F Y 0.00000 20160831 MD CA 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
116528915 11652891 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK 21817 5 MG SOLUTION FOR INJECTION
116528915 11652891 2 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK 21817 SOLUTION FOR INJECTION
116528915 11652891 3 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK 21817 SOLUTION FOR INJECTION
116528915 11652891 4 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK 21817 SOLUTION FOR INJECTION
116528915 11652891 5 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK 21817 SOLUTION FOR INJECTION
116528915 11652891 6 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK 21817 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116528915 11652891 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
116528915 11652891 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116528915 11652891 Arthralgia
116528915 11652891 Blood calcium increased
116528915 11652891 Fall
116528915 11652891 Lower limb fracture
116528915 11652891 Parathyroid disorder

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
116528915 11652891 1 20090313 0
116528915 11652891 2 20100422 0
116528915 11652891 3 20110420 0
116528915 11652891 4 20120423 0
116528915 11652891 5 20130618 0
116528915 11652891 6 20140528 0