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
118529262 11852926 2 F 20151211 20160712 20151218 20160718 PER PHEH2015US026091 NOVARTIS 13.28 YR F Y 0.00000 20160718 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
118529262 11852926 1 PS AFINITOR EVEROLIMUS 1 Oral 5 MG, QD U 22334 5 MG TABLET QD
118529262 11852926 2 SS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD U 22334 10 MG TABLET QD
118529262 11852926 3 SS ZYPREXA OLANZAPINE 1 Unknown U 0
118529262 11852926 4 C CLONIDINE HYDROCHLORIDE. CLONIDINE HYDROCHLORIDE 1 Unknown U 0
118529262 11852926 5 C MELATONIN MELATONIN 1 Unknown U 0
118529262 11852926 6 C OXTELLAR 2 Unknown U 0
118529262 11852926 7 C DISOTAT 2 Unknown UNK, PRN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118529262 11852926 1 Astrocytoma, low grade
118529262 11852926 2 Ganglioglioma
118529262 11852926 3 Product used for unknown indication
118529262 11852926 4 Product used for unknown indication
118529262 11852926 5 Product used for unknown indication
118529262 11852926 6 Product used for unknown indication
118529262 11852926 7 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118529262 11852926 Therapeutic response unexpected
118529262 11852926 Weight 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
118529262 11852926 2 20150919 0