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
121671972 12167197 2 F 20160304 20160802 20160310 20160805 PER PHEH2016US005660 NOVARTIS 33.70 YR M Y 0.00000 20160805 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
121671972 12167197 1 PS AFINITOR EVEROLIMUS 1 Oral 1 DF, Q D(2-10 MG) U 22334 1 DF TABLET QD
121671972 12167197 2 C TEGRETOL CARBAMAZEPINE 1 Unknown N 0
121671972 12167197 3 C LAMICTAL LAMOTRIGINE 1 Unknown U 0
121671972 12167197 4 C VITAMAN MINERALSVITAMINS 1 Unknown U 0
121671972 12167197 5 C BENZOTROPINE BENZTROPINE 1 Unknown U 0
121671972 12167197 6 C SINGULAIR MONTELUKAST SODIUM 1 Unknown U 0
121671972 12167197 7 C ATENOLOL. ATENOLOL 1 Unknown U 0
121671972 12167197 8 C ATARAX HYDROXYZINEHYDROXYZINE HYDROCHLORIDE 1 Unknown U 0
121671972 12167197 9 C MELATONIN MELATONIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121671972 12167197 1 Angiomyolipoma
121671972 12167197 2 Product used for unknown indication
121671972 12167197 4 Product used for unknown indication
121671972 12167197 5 Product used for unknown indication
121671972 12167197 6 Product used for unknown indication
121671972 12167197 7 Product used for unknown indication
121671972 12167197 8 Product used for unknown indication
121671972 12167197 9 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121671972 12167197 Blood cholesterol increased
121671972 12167197 Decreased appetite

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
121671972 12167197 1 20141124 0