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
127711411 12771141 1 I 20160913 20160920 20160922 20160922 EXP PHHY2016NL129964 NOVARTIS 85.85 YR F Y 0.00000 20160922 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
127711411 12771141 1 PS ZOMETA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 4 MG/ 100ML, Q5W (1 X PER 5 WEEKS) D 21223 4 MG SOLUTION FOR INFUSION
127711411 12771141 2 SS ZOMETA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) UNK D S0160 21223 SOLUTION FOR INFUSION
127711411 12771141 3 SS ZOMETA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) UNK D S0160 21223 SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127711411 12771141 1 Breast cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
127711411 12771141 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127711411 12771141 Death
127711411 12771141 Inappropriate schedule of drug administration

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
127711411 12771141 2 20160713 0
127711411 12771141 3 20160817 0