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
126897892 12689789 2 F 201603 20160906 20160826 20160912 EXP PHHY2016MX116341 NOVARTIS 84.70 YR F Y 85.00000 KG 20160912 CN COUNTRY NOT SPECIFIED MX

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
126897892 12689789 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 10 CM2, QD 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
126897892 12689789 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 10 CM2, QD 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
126897892 12689789 3 C ADALAT NIFEDIPINE 1 Oral 1 DF, QD 0 1 DF TABLET QD
126897892 12689789 4 C EVISTA RALOXIFENE HYDROCHLORIDE 1 Unknown U 0
126897892 12689789 5 C EBIXA MEMANTINE HYDROCHLORIDE 1 Oral 1 DF, QD 0 1 DF TABLET QD
126897892 12689789 6 C NIFEDIPINE. NIFEDIPINE 1 Oral 2 DF, QD 0 2 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126897892 12689789 1 Memory impairment
126897892 12689789 2 Senile dementia
126897892 12689789 3 Hypertension
126897892 12689789 4 Product used for unknown indication
126897892 12689789 5 Memory impairment
126897892 12689789 6 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126897892 12689789 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126897892 12689789 Fall
126897892 12689789 Femur fracture

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
126897892 12689789 1 201603 201605 0
126897892 12689789 3 2014 0
126897892 12689789 5 2012 0
126897892 12689789 6 2012 0