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
127915631 12791563 1 I 20160629 20160712 20160929 20160929 PER US-ASTRAZENECA-2016SE76723 ASTRAZENECA 32785.00 DY F Y 0.00000 20160929 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
127915631 12791563 1 PS FASLODEX FULVESTRANT 1 Intramuscular 250.0MG UNKNOWN U 21344 250 MG INJECTION
127915631 12791563 2 SS FASLODEX FULVESTRANT 1 Intramuscular UNKNOWN U 21344 INJECTION
127915631 12791563 3 SS IBRANCE PALBOCICLIB 1 Oral 75.0MG UNKNOWN U 0 75 MG CAPSULE
127915631 12791563 4 SS IBRANCE PALBOCICLIB 1 Oral 75.0MG UNKNOWN U 0 75 MG CAPSULE

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127915631 12791563 Decreased appetite
127915631 12791563 Diarrhoea
127915631 12791563 Weight decreased

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
127915631 12791563 1 201509 0
127915631 12791563 2 20160629 0
127915631 12791563 3 201509 0
127915631 12791563 4 201510 0