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
117798673 11779867 3 F 20160817 20151125 20160818 EXP US-GLAXOSMITHKLINE-US2015GSK166829 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
117798673 11779867 1 PS LAMOTRIGINE. LAMOTRIGINE 1 UNK, U U 20241
117798673 11779867 2 SS LAMICTAL LAMOTRIGINE 1 UNK, U N 0 PROLONGED-RELEASE TABLET
117798673 11779867 3 SS KEPPRA XR LEVETIRACETAM 1 UNK, U N 0
117798673 11779867 4 C FENUGREEK FENUGREEK SEED 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117798673 11779867 1 Product used for unknown indication
117798673 11779867 2 Product used for unknown indication
117798673 11779867 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
117798673 11779867 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117798673 11779867 Drug ineffective
117798673 11779867 Exposure during breast feeding
117798673 11779867 Exposure during pregnancy
117798673 11779867 Seizure
117798673 11779867 Suppressed lactation

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

no results found

Therapies reported

no results found