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
100808473 10080847 3 F 201308 20160808 20140416 20160811 EXP PHHY2014ZA044880 NOVARTIS 71.68 YR F Y 0.00000 20160811 MD ZA 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
100808473 10080847 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 1 DF, Q12MO 21817 1 DF SOLUTION FOR INJECTION
100808473 10080847 2 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 1 DF, UNK 21817 1 DF SOLUTION FOR INJECTION
100808473 10080847 3 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 1 DF, Q12MO 21817 1 DF SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100808473 10080847 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
100808473 10080847 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100808473 10080847 Anal fissure
100808473 10080847 Back pain
100808473 10080847 Bronchitis
100808473 10080847 Lung infection
100808473 10080847 Pneumonia
100808473 10080847 Subcutaneous abscess

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
100808473 10080847 1 2012 0
100808473 10080847 2 201311 0
100808473 10080847 3 2015 0