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
116183213 11618321 3 F 20150917 20160721 20151012 20160726 PER PHEH2015US020159 NOVARTIS 18.51 YR F Y 0.00000 20160726 CN COUNTRY NOT SPECIFIED 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
116183213 11618321 1 PS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD (ONCE DAILY) 22334 10 MG QD
116183213 11618321 2 SS AFINITOR EVEROLIMUS 1 22334
116183213 11618321 3 C LAMICTAL LAMOTRIGINE 1 Unknown Y 0
116183213 11618321 4 C LAMICTAL LAMOTRIGINE 1 Unknown DOSE DECREASED Y 0
116183213 11618321 5 C LEXAPRO ESCITALOPRAM OXALATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116183213 11618321 1 Ganglioglioma
116183213 11618321 2 Astrocytoma, low grade
116183213 11618321 3 Product used for unknown indication
116183213 11618321 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
116183213 11618321 Cough
116183213 11618321 Stomatitis
116183213 11618321 Upper respiratory tract infection

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
116183213 11618321 1 20140201 0
116183213 11618321 4 20160713 0