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
127877681 12787768 1 I 2015 20160921 20160928 20160928 EXP US-GLAXOSMITHKLINE-US2016GSK139078 GLAXOSMITHKLINE 0.00 F Y 39.91000 KG 20160928 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
127877681 12787768 1 PS NICODERM CQ NICOTINE 1 UNK N 20165 TRANSDERMAL PATCH
127877681 12787768 2 SS ALBUTEROL. ALBUTEROL 1 N 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127877681 12787768 1 Product used for unknown indication
127877681 12787768 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127877681 12787768 HO
127877681 12787768 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127877681 12787768 Adverse event
127877681 12787768 Aphasia
127877681 12787768 Atrial fibrillation
127877681 12787768 Cardiac disorder
127877681 12787768 Catheterisation cardiac
127877681 12787768 Condition aggravated
127877681 12787768 Drug hypersensitivity
127877681 12787768 Heart rate increased
127877681 12787768 Hospitalisation
127877681 12787768 Hypertension

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
127877681 12787768 1 2015 0