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
126107671 12610767 1 I 20160725 20160801 20160801 EXP US-AMGEN-USASP2016096917 AMGEN 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
126107671 12610767 1 PS XGEVA DENOSUMAB 1 Unknown UNK U 125320 UNKNOWN FORMULATION
126107671 12610767 2 SS IBRANCE PALBOCICLIB 1 Unknown UNK 0
126107671 12610767 3 SS FASLODEX FULVESTRANT 1 Unknown UNK 0
126107671 12610767 4 C FEMARA LETROZOLE 1 UNK 0
126107671 12610767 5 C AREDIA PAMIDRONATE DISODIUM 1 UNK 0
126107671 12610767 6 C INSULIN INSULIN NOS 1 0
126107671 12610767 7 C METFORMIN METFORMIN HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126107671 12610767 1 Product used for unknown indication
126107671 12610767 2 Product used for unknown indication
126107671 12610767 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126107671 12610767 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126107671 12610767 Blood count abnormal
126107671 12610767 Blood oestrogen decreased
126107671 12610767 Depression
126107671 12610767 Diarrhoea
126107671 12610767 Dry skin
126107671 12610767 Fatigue
126107671 12610767 Hepatic neoplasm

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
126107671 12610767 3 2013 0
126107671 12610767 4 2015 0