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
127866991 12786699 1 I 20160920 20160927 20160927 EXP US-ASTRAZENECA-2016SF01134 ASTRAZENECA 0.00 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
127866991 12786699 1 PS FASLODEX FULVESTRANT 1 Intramuscular U 21344 INJECTION
127866991 12786699 2 SS IBRANCE PALBOCICLIB 1 Oral U 0 CAPSULE

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127866991 12786699 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127866991 12786699 Hepatic enzyme increased
127866991 12786699 Malignant neoplasm progression
127866991 12786699 Metastases to bone
127866991 12786699 Metastases to liver
127866991 12786699 Tumour marker increased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found