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
126915961 12691596 1 I 20121013 20121016 20160826 20160826 EXP JP-GLAXOSMITHKLINE-B0839306A GLAXOSMITHKLINE 51.00 YR M Y 0.00000 20160826 CN JP JP

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
126915961 12691596 1 PS LAMOTRIGINE. LAMOTRIGINE 1 Oral 50 MG, QD 1950 MG 20241 50 MG TABLET QD
126915961 12691596 2 SS PREDNISOLONE. PREDNISOLONE 1 Oral 400 MG, BID 0 400 MG BID
126915961 12691596 3 SS ARIPIPRAZOLE. ARIPIPRAZOLE 1 Oral 12 MG, BID 0 12 MG BID
126915961 12691596 4 SS AKINETON BIPERIDEN HYDROCHLORIDE 1 Oral 0 1 MG TABLET BID
126915961 12691596 5 C UNKNOWN DRUG UNSPECIFIED INGREDIENT 1 Unknown U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126915961 12691596 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126915961 12691596 Erythema
126915961 12691596 Pruritus
126915961 12691596 Rash
126915961 12691596 Swelling face

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
126915961 12691596 1 20120904 20121014 0