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
126655611 12665561 1 I 20160803 20160818 20160818 EXP US-GLAXOSMITHKLINE-US2016GSK113380 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160818 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
126655611 12665561 1 PS WELLBUTRIN BUPROPION HYDROCHLORIDE 1 U 18644
126655611 12665561 2 SS LAMICTAL LAMOTRIGINE 1 U 0
126655611 12665561 3 SS ASPIRIN. ASPIRIN 1 U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126655611 12665561 Abdominal pain upper
126655611 12665561 Drug hypersensitivity
126655611 12665561 Rash

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found