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
119757135 11975713 5 F 20150127 20160907 20160129 20160913 PER PHEH2015US002200 NOVARTIS 11.03 YR F Y 0.00000 20160913 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
119757135 11975713 1 PS AFINITOR EVEROLIMUS 1 Oral 5 MG, QD Y 22334 5 MG TABLET QD
119757135 11975713 2 C RAPAMYCIN SIROLIMUS 1 Unknown U 0 CREAM
119757135 11975713 3 C LYSINE LYSINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119757135 11975713 1 Brain neoplasm benign
119757135 11975713 2 Product used for unknown indication
119757135 11975713 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119757135 11975713 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119757135 11975713 Blood cholesterol increased
119757135 11975713 Cough
119757135 11975713 Pneumonia
119757135 11975713 Pyrexia
119757135 11975713 Respiratory tract infection viral
119757135 11975713 Stomatitis

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
119757135 11975713 1 20140410 0