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
113687052 11368705 2 F 20150731 20160914 20150812 20160917 PER PHEH2015US014993 NOVARTIS 13.68 YR M Y 0.00000 20160917 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
113687052 11368705 1 PS AFINITOR EVEROLIMUS 1 Oral 10.0 MG, QD 22334 10 MG QD
113687052 11368705 2 C LAMICTAL LAMOTRIGINE 1 Unknown U 0
113687052 11368705 3 C DIASTAT /01384601/ 2 Unknown UNK UNK, PRN U 0
113687052 11368705 4 C MAGIC MOUTHWASH DIPHENHYDRAMINE HYDROCHLORIDELIDOCAINE HYDROCHLORIDENYSTATIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113687052 11368705 1 Brain neoplasm
113687052 11368705 2 Product used for unknown indication
113687052 11368705 3 Product used for unknown indication
113687052 11368705 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
113687052 11368705 Abnormal behaviour
113687052 11368705 Rash

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
113687052 11368705 1 20121114 0