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
125442681 12544268 1 I 20160707 20160711 20160711 EXP PHHY2016NL094578 NOVARTIS 0.00 F Y 0.00000 20160711 CN COUNTRY NOT SPECIFIED NL

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
125442681 12544268 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, (ONCE PER 52 WEEKS) 16GA0193 21817 5 MG
125442681 12544268 2 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, (ONCE PER 52 WEEKS) 16GH0085 21817 5 MG
125442681 12544268 3 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, (ONCE PER 52 WEEKS) 16HB0109A 21817 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125442681 12544268 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
125442681 12544268 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125442681 12544268 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
125442681 12544268 1 20130822 0
125442681 12544268 2 20140723 0
125442681 12544268 3 20150728 0