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
122132143 12213214 3 F 20150223 20160823 20160328 20160830 EXP PHHY2016DE017028 NOVARTIS 0.00 E F Y 94.00000 KG 20160830 MD DE DE

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
122132143 12213214 1 PS AFINITOR EVEROLIMUS 1 Oral 5 MG, QD 490 MG 22334 5 MG TABLET QD
122132143 12213214 2 C EXEMESTANE. EXEMESTANE 1 Oral 25 MG, QD 2475.47803 MG 0 25 MG QD
122132143 12213214 3 C ZOMETA ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) EVERY 4 WEEKS Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122132143 12213214 1 Breast cancer metastatic
122132143 12213214 2 Breast cancer metastatic
122132143 12213214 3 Metastases to bone

Outcome of event

Event ID CASEID OUTC COD
122132143 12213214 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122132143 12213214 Bone swelling
122132143 12213214 Complication associated with device
122132143 12213214 Feeding disorder
122132143 12213214 Lymphadenopathy
122132143 12213214 Pain

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
122132143 12213214 1 20141117 20150222 0
122132143 12213214 2 20141117 0
122132143 12213214 3 2010 0