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
124036102 12403610 2 F 20160511 20160805 20160525 20160810 PER PHEH2016US012890 NOVARTIS 11.18 YR M Y 0.00000 20160810 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
124036102 12403610 1 PS AFINITOR EVEROLIMUS 1 Oral 5 MG, QD 22334 5 MG TABLET QD
124036102 12403610 2 C RISPERDAL RISPERIDONE 1 Unknown U 0
124036102 12403610 3 C VITAMIN B6 PYRIDOXINE HYDROCHLORIDE 1 Unknown U 0
124036102 12403610 4 C DILANTIN PHENYTOIN 1 Unknown U 0
124036102 12403610 5 C TENEX GUANFACINE HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124036102 12403610 1 Brain neoplasm benign
124036102 12403610 2 Product used for unknown indication
124036102 12403610 3 Product used for unknown indication
124036102 12403610 4 Product used for unknown indication
124036102 12403610 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124036102 12403610 Anal incontinence
124036102 12403610 Urinary incontinence
124036102 12403610 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
124036102 12403610 1 20160511 0