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
127663381 12766338 1 I 20120817 20120821 20160921 20160921 EXP PHHY2012CA073836 NOVARTIS 73.59 YR M Y 0.00000 20160921 CN 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
127663381 12766338 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK D 21817 5 MG SOLUTION FOR INJECTION
127663381 12766338 2 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK D 21817 SOLUTION FOR INJECTION
127663381 12766338 3 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK D 21817 SOLUTION FOR INJECTION
127663381 12766338 4 SS ACLASTA ZOLEDRONIC ACID 1 Unknown UNK D 21817 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127663381 12766338 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
127663381 12766338 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127663381 12766338 Back pain
127663381 12766338 Fall
127663381 12766338 Fracture
127663381 12766338 Glomerular filtration rate decreased

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
127663381 12766338 1 20120814 0
127663381 12766338 2 20130914 0
127663381 12766338 3 20140920 0
127663381 12766338 4 20151003 0