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
114190502 11419050 2 F 20150521 20160810 20150826 20160812 PER PHEH2015US009990 NOVARTIS 55.68 YR M Y 0.00000 20160812 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
114190502 11419050 1 PS AFINITOR EVEROLIMUS 1 Oral 5 MG, QD U 22334 5 MG QD
114190502 11419050 2 C ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown U 0
114190502 11419050 3 C RAPAMYCIN SIROLIMUS 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114190502 11419050 1 Angiomyolipoma
114190502 11419050 2 Product used for unknown indication
114190502 11419050 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
114190502 11419050 Dermatitis acneiform
114190502 11419050 Oral pain
114190502 11419050 Pain in jaw
114190502 11419050 Stomatitis
114190502 11419050 Tooth abscess

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
114190502 11419050 1 20150423 0