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
127006761 12700676 1 I 20160324 20160405 20160830 20160830 PER US-SA-2016SA070093 AVENTIS 86.00 YR E F Y 128.00000 KG 20160830 CN 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
127006761 12700676 1 PS MULTAQ DRONEDARONE 1 Unknown Y 5397752 22425 400 MG TABLET BID
127006761 12700676 2 C ATORVASTATIN ATORVASTATIN 1 0 10 MG QD
127006761 12700676 3 C TORASEMIDE TORSEMIDE 1 0 5 MG QD
127006761 12700676 4 C ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 0 5 MG /wk
127006761 12700676 5 C ELIQUIS APIXABAN 1 0 2.5 MG BID
127006761 12700676 6 C METOPROLOL. METOPROLOL 1 25MG 0 .5 DF TABLET QD
127006761 12700676 7 C LOSARTAN. LOSARTAN 1 0 100 MG QD
127006761 12700676 8 C AMLODIPINE BESILATE AMLODIPINE BESYLATE 1 0 2.5 MG QD
127006761 12700676 9 C CENTRUM SILVER MINERALSVITAMINS 1 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127006761 12700676 1 Cardiac fibrillation
127006761 12700676 3 Polyuria
127006761 12700676 4 Osteoporosis
127006761 12700676 5 Anticoagulant therapy
127006761 12700676 7 Blood pressure measurement

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127006761 12700676 Contusion
127006761 12700676 Fall
127006761 12700676 Malaise
127006761 12700676 Nausea
127006761 12700676 Syncope

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
127006761 12700676 1 20160324 20160331 0