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
125233861 12523386 1 I 20160601 20160607 20160703 20160703 PER US-ASTRAZENECA-2016SE61720 ASTRAZENECA 24003.00 DY F Y 62.60000 KG 20160703 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
125233861 12523386 1 PS ARIMIDEX ANASTROZOLE 1 Oral Y 20541 TABLET
125233861 12523386 2 SS FASLODEX FULVESTRANT 1 Intramuscular U U 21344 INJECTION
125233861 12523386 3 SS FASLODEX FULVESTRANT 1 Intramuscular U 0 INJECTION
125233861 12523386 4 SS IBRANCE PALBOCICLIB 1 Oral 250 MG M78671 0 125 MG CAPSULE QD
125233861 12523386 5 C LEXAPRO ESCITALOPRAM OXALATE 1 0 10 MG QD
125233861 12523386 6 C LEXAPRO ESCITALOPRAM OXALATE 1 0 10 MG QD
125233861 12523386 7 C AMOUR 2 60.0MG UNKNOWN 0 60 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125233861 12523386 2 Antioestrogen therapy
125233861 12523386 4 Neoplasm malignant
125233861 12523386 5 Anxiety
125233861 12523386 6 Depression
125233861 12523386 7 Thyroid disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125233861 12523386 Feeling hot
125233861 12523386 Headache
125233861 12523386 Hypersensitivity
125233861 12523386 Irritability
125233861 12523386 Menopause
125233861 12523386 Nausea
125233861 12523386 Osteoporosis
125233861 12523386 Yawning

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
125233861 12523386 2 20160531 0
125233861 12523386 4 20160531 0