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
127460121 12746012 1 I 20160825 20160831 20160915 20160915 PER US-GLAXOSMITHKLINE-US2016127255 GLAXOSMITHKLINE 22.00 YR F Y 0.00000 20160915 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
127460121 12746012 1 PS NICODERM CQ NICOTINE 1 21 MG, UNK N 1601459 20165 21 MG TRANSDERMAL PATCH

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127460121 12746012 1 Smoking cessation therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127460121 12746012 Anxiety
127460121 12746012 Application site erythema
127460121 12746012 Application site pruritus
127460121 12746012 Application site reaction
127460121 12746012 Chest discomfort
127460121 12746012 Hyperchlorhydria
127460121 12746012 Irritability
127460121 12746012 Nausea
127460121 12746012 Nervousness
127460121 12746012 Product adhesion issue
127460121 12746012 Product quality issue

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
127460121 12746012 1 20160825 20160831 0