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
126091681 12609168 1 I 20160725 20160731 20160731 EXP PHEH2016US018573 NOVARTIS 0.00 F Y 0.00000 20160801 CN US US

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
126091681 12609168 1 PS FEMARA LETROZOLE 1 Unknown 20726
126091681 12609168 2 SS AREDIA PAMIDRONATE DISODIUM 1 Unknown U 0
126091681 12609168 3 SS XGEVA DENOSUMAB 1 Unknown U 0
126091681 12609168 4 SS FASLODEX FULVESTRANT 1 Unknown U 0
126091681 12609168 5 C INSULIN INSULIN NOS 1 Unknown U 0
126091681 12609168 6 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126091681 12609168 1 Product used for unknown indication
126091681 12609168 2 Product used for unknown indication
126091681 12609168 3 Product used for unknown indication
126091681 12609168 4 Product used for unknown indication
126091681 12609168 5 Diabetes mellitus
126091681 12609168 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126091681 12609168 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126091681 12609168 Depression
126091681 12609168 Dry skin
126091681 12609168 Fatigue
126091681 12609168 Full blood count decreased
126091681 12609168 Hepatic neoplasm
126091681 12609168 Metastasis

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
126091681 12609168 1 2015 0
126091681 12609168 4 2013 0