The Safety Rates Drug Report

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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
122009824 12200982 4 F 20160312 20160630 20160322 20160707 PER PHEH2016US006367 NOVARTIS 15.78 YR M Y 0.00000 20160707 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
122009824 12200982 1 PS AFINITOR EVEROLIMUS 1 Oral 5 MG, QD 22334 5 MG QD
122009824 12200982 2 C CARBATROL CARBAMAZEPINE 1 Unknown U 0
122009824 12200982 3 C RAPAMUNE SIROLIMUS 1 Unknown U 0
122009824 12200982 4 C ISOTRETINOIN ISOTRETINOIN 1 Unknown U 0
122009824 12200982 5 C MULTI VITAMIN VITAMINS 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122009824 12200982 1 Astrocytoma, low grade
122009824 12200982 2 Product used for unknown indication
122009824 12200982 3 Product used for unknown indication
122009824 12200982 4 Product used for unknown indication
122009824 12200982 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122009824 12200982 Constipation
122009824 12200982 Fibroma
122009824 12200982 Rash
122009824 12200982 Therapeutic response unexpected

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
122009824 12200982 1 20160310 0