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
114244792 11424479 2 F 20150928 20150827 20160830 PER US-SA-2015SA053744 AVENTIS 0.00 A F Y 0.00000 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
114244792 11424479 1 PS MULTAQ DRONEDARONE 1 Unknown U UNKNOWN 22425
114244792 11424479 2 C DIGOXIN. DIGOXIN 1 2 TABLETS IN THE AM AND PM MWF AND 1 TABLET THE OTHER 4 DAYS 0 .125 MG TABLET
114244792 11424479 3 C LOVASTATIN. LOVASTATIN 1 0 QD
114244792 11424479 4 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
114244792 11424479 5 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0
114244792 11424479 6 C XOPENEX LEVALBUTEROL HYDROCHLORIDE 1 Respiratory (inhalation) NEBULIZER FORM 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114244792 11424479 1 Atrial fibrillation
114244792 11424479 4 Asthma
114244792 11424479 5 Asthma
114244792 11424479 6 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
114244792 11424479 Blood pressure increased
114244792 11424479 Cough
114244792 11424479 Heart rate increased

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
114244792 11424479 1 20130506 0