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
125822041 12582204 1 I 2011 20160614 20160722 20160722 PER US-ASTRAZENECA-2016SE66057 ASTRAZENECA 64.00 YR F Y 68.00000 KG 20160722 US 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
125822041 12582204 1 PS ANASTROZOLE. ANASTROZOLE 1 Oral 0 1 MG TABLET QD
125822041 12582204 2 SS METOPROLOL ER METOPROLOL SUCCINATE 1 Oral 0 50 MG MODIFIED-RELEASE TABLET QD
125822041 12582204 3 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral 0 20 MG QD
125822041 12582204 4 C ZOLPIDEM ZOLPIDEMOLPIDEM TARTRATE 1 Oral 0 .5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125822041 12582204 1 Breast cancer female
125822041 12582204 2 Blood pressure increased
125822041 12582204 3 Gastrooesophageal reflux disease
125822041 12582204 4 Sleep disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125822041 12582204 Fatigue
125822041 12582204 Hot flush
125822041 12582204 Hyperhidrosis
125822041 12582204 Insomnia
125822041 12582204 Listless
125822041 12582204 Nausea

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
125822041 12582204 1 201102 201606 0
125822041 12582204 2 2013 0
125822041 12582204 3 2013 0
125822041 12582204 4 2013 0