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
125224902 12522490 2 F 20160623 20160630 20160701 20160705 EXP PHHY2016CO090707 NOVARTIS 72.67 YR F Y 65.00000 KG 20160705 CN COUNTRY NOT SPECIFIED CO

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
125224902 12522490 1 PS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 22334 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125224902 12522490 1 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
125224902 12522490 OT
125224902 12522490 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125224902 12522490 Abdominal pain upper
125224902 12522490 Back pain
125224902 12522490 Gait disturbance
125224902 12522490 General physical health deterioration
125224902 12522490 Headache
125224902 12522490 Hepatic cirrhosis
125224902 12522490 Malaise
125224902 12522490 Malignant neoplasm progression
125224902 12522490 Metastases to bone
125224902 12522490 Pain
125224902 12522490 Procedural headache
125224902 12522490 Procedural pain
125224902 12522490 Respiratory arrest
125224902 12522490 Tumour pain

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
125224902 12522490 1 20160510 0