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
126306472 12630647 2 F 20160815 20160808 20160823 EXP US-PFIZER INC-2016367140 PFIZER 47.00 YR F Y 0.00000 20160823 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
126306472 12630647 1 PS IBRANCE PALBOCICLIB 1 Oral 125 MG, DAILY (1 CAPSULE) 207103 125 MG CAPSULE
126306472 12630647 2 SS LETROZOLE. LETROZOLE 1 UNK U 0
126306472 12630647 3 SS ZOLADEX GOSERELIN ACETATE 1 UNK U 0
126306472 12630647 4 C FASLODEX FULVESTRANT 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126306472 12630647 1 Breast cancer metastatic
126306472 12630647 2 Breast cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
126306472 12630647 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126306472 12630647 Feeling abnormal
126306472 12630647 Hypoaesthesia
126306472 12630647 Mood altered
126306472 12630647 Peripheral swelling

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
126306472 12630647 1 20160722 0
126306472 12630647 2 20160722 0