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
127454582 12745458 2 F 201609 20160922 20160915 20160927 PER US-PFIZER INC-2016427125 PFIZER 52.00 YR F Y 0.00000 20160927 OT 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
127454582 12745458 1 PS IBRANCE PALBOCICLIB 1 Oral 125 MG, CYCLIC (DAILY FOR DAYS 1-21 EVERY 28 DAYS) U 207103 125 MG CAPSULE
127454582 12745458 2 SS FASLODEX FULVESTRANT 1 2 INJECTIONS U 0 INJECTION
127454582 12745458 3 C VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 UNK 0
127454582 12745458 4 C TAMOXIFEN TAMOXIFEN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127454582 12745458 1 Neoplasm malignant

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127454582 12745458 Arthralgia
127454582 12745458 Fatigue
127454582 12745458 Gingival pain
127454582 12745458 Injection site swelling
127454582 12745458 Nausea
127454582 12745458 Peripheral swelling
127454582 12745458 Pruritus
127454582 12745458 Rash

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
127454582 12745458 1 201608 0
127454582 12745458 2 20160901 0