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
119825673 11982567 3 F 20141219 20160530 20160201 20160706 EXP PHHY2015FR075459 NOVARTIS 0.00 E M Y 0.00000 20160706 MD FR FR

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
119825673 11982567 1 PS AFINITOR EVEROLIMUS 1 Unknown 5 MG, QD U 22334 5 MG QD
119825673 11982567 2 SS AFINITOR EVEROLIMUS 1 Unknown UNK U 22334

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119825673 11982567 1 Renal cancer

Outcome of event

Event ID CASEID OUTC COD
119825673 11982567 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119825673 11982567 Arthralgia
119825673 11982567 Asthenia
119825673 11982567 Decreased appetite
119825673 11982567 Dysuria
119825673 11982567 Herpes zoster
119825673 11982567 Lung disorder
119825673 11982567 Palmar-plantar erythrodysaesthesia syndrome
119825673 11982567 Pruritus

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
119825673 11982567 1 201411 2015 0
119825673 11982567 2 2015 0