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
117135233 11713523 3 F 20141222 20160727 20151109 20160801 PER PHEH2015US000846 NOVARTIS 8.82 YR F Y 0.00000 20160801 MD 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
117135233 11713523 1 PS AFINITOR EVEROLIMUS 1 Oral Y U 22334
117135233 11713523 2 SS AFINITOR EVEROLIMUS 1 Oral 7.5 MG, QD Y U 22334 7.5 MG QD
117135233 11713523 3 C MULTI VITAMIN VITAMINS 1 Unknown U 0
117135233 11713523 4 C RISPERDAL RISPERIDONE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117135233 11713523 1 Astrocytoma, low grade
117135233 11713523 2 Ganglioglioma
117135233 11713523 3 Product used for unknown indication
117135233 11713523 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
117135233 11713523 Dehydration
117135233 11713523 Eating disorder
117135233 11713523 Gastroenteritis viral
117135233 11713523 Malaise
117135233 11713523 Pyrexia
117135233 11713523 Varicella
117135233 11713523 Viral infection
117135233 11713523 Vomiting

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
117135233 11713523 1 20141107 20141222 0
117135233 11713523 2 20150108 0