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
127411971 12741197 1 I 20160912 20160912 20160914 20160914 EXP PHHY2016NL125572 NOVARTIS 72.18 YR M Y 0.00000 20160914 CN NL 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
127411971 12741197 1 PS ZOMETA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 4 MG/100 ML (ONCE PER 6 WEEKS,) U 21223 4 MG SOLUTION FOR INFUSION
127411971 12741197 2 SS ZOMETA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) UNK UKN, UNK U S0098 21223 SOLUTION FOR INFUSION
127411971 12741197 3 SS ZOMETA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) UNK UKN, UNK U S0160 21223 SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127411971 12741197 1 Prostate cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
127411971 12741197 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127411971 12741197 Inappropriate schedule of drug administration
127411971 12741197 Myocardial infarction

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
127411971 12741197 2 20140117 0
127411971 12741197 3 20160802 0