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
101929602 10192960 2 F 20151228 20140523 20151231 EXP PHHY2013MX119238 NOVARTIS 0.00 F Y 0.00000 20160101 CN COUNTRY NOT SPECIFIED MX

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
101929602 10192960 1 PS ZOMETA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 4 MG, ANNUALLY 21223 4 MG SOLUTION FOR INFUSION
101929602 10192960 2 C PROZAC FLUOXETINE HYDROCHLORIDE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101929602 10192960 1 Osteoporosis
101929602 10192960 2 Sleep disorder

Outcome of event

Event ID CASEID OUTC COD
101929602 10192960 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
101929602 10192960 Breast cancer
101929602 10192960 Metastases to liver
101929602 10192960 Metastases to lung
101929602 10192960 Metastases to pleura
101929602 10192960 Product use issue

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
101929602 10192960 1 201009 0