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
127792471 12779247 1 I 201602 20160919 20160926 20160926 EXP US-ASTRAZENECA-2016SF00551 ASTRAZENECA 788.00 MON F Y 78.00000 KG 20160926 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
127792471 12779247 1 PS ANASTROZOLE. ANASTROZOLE 1 Oral Y U 20541 TABLET
127792471 12779247 2 SS FASLODEX FULVESTRANT 1 Intramuscular 0 500 MG INJECTION /month
127792471 12779247 3 SS IBRANCE PALBOCICLIB 1 Oral 100.0MG UNKNOWN Y U 0 100 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127792471 12779247 1 Breast cancer
127792471 12779247 2 Breast cancer
127792471 12779247 3 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
127792471 12779247 HO
127792471 12779247 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127792471 12779247 Arthralgia
127792471 12779247 Contusion
127792471 12779247 Cough
127792471 12779247 Facial spasm
127792471 12779247 Injection site pruritus
127792471 12779247 Oropharyngeal discomfort
127792471 12779247 Ovarian disorder
127792471 12779247 Pain in extremity
127792471 12779247 Platelet count decreased
127792471 12779247 Rash
127792471 12779247 Tumour marker increased

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
127792471 12779247 1 2012 0
127792471 12779247 2 201603 0