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
111137173 11113717 3 F 201503 20160705 20150514 20160708 EXP JP-GLAXOSMITHKLINE-JP2015JPN063339 GLAXOSMITHKLINE 46.63 YR F Y 56.00000 KG 20160708 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
111137173 11113717 1 PS LAMICTAL LAMOTRIGINE 1 Oral 25 MG, QD 1300 MG Y 20241 25 MG TABLET QD
111137173 11113717 2 SS LAMICTAL LAMOTRIGINE 1 Oral 50 MG, QD 1300 MG Y 20241 50 MG TABLET QD
111137173 11113717 3 SS LAMICTAL LAMOTRIGINE 1 Oral 100 MG, QD 1300 MG Y 20241 100 MG TABLET QD
111137173 11113717 4 C JZOLOFT SERTRALINE HYDROCHLORIDE 1 50 MG, 1D 0 50 MG QD
111137173 11113717 5 C JZOLOFT SERTRALINE HYDROCHLORIDE 1 25 MG, 1D 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111137173 11113717 1 Bipolar disorder

Outcome of event

Event ID CASEID OUTC COD
111137173 11113717 HO
111137173 11113717 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
111137173 11113717 Drug eruption
111137173 11113717 Rash
111137173 11113717 Skin disorder

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
111137173 11113717 1 20150130 20150211 0
111137173 11113717 2 20150212 20150226 0
111137173 11113717 3 20150227 20150303 0