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
125205001 12520500 1 I 20160627 20160701 20160701 EXP PHHY2016CA089023 NOVARTIS 0.00 F Y 0.00000 20160701 CN COUNTRY NOT SPECIFIED 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
125205001 12520500 1 PS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK 21817 5 MG SOLUTION FOR INJECTION
125205001 12520500 2 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK 21817 5 MG SOLUTION FOR INJECTION
125205001 12520500 3 SS ACLASTA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK 21817 5 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125205001 12520500 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
125205001 12520500 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125205001 12520500 Feeling abnormal
125205001 12520500 Malaise

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
125205001 12520500 1 20130128 0
125205001 12520500 2 20140212 0
125205001 12520500 3 20150416 0