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
126894871 12689487 1 I 20160816 20160826 20160826 EXP DE-BFARM-16268404 DE-GLAXOSMITHKLINE-DE2016GSK123515 GLAXOSMITHKLINE 2.00 WK F Y 0.00000 20160826 OT DE DE

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
126894871 12689487 1 PS LAMICTAL LAMOTRIGINE 1 Transmammary 50 MG, BID U 20764 50 MG CHEWABLE TABLET BID
126894871 12689487 2 SS LEVETIRACETAM. LEVETIRACETAM 1 Transmammary 4000 MG, QD U 0 4000 MG QD
126894871 12689487 3 SS LEVETIRACETAM. LEVETIRACETAM 1 4500 UNK, UNK U 0 4500 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126894871 12689487 1 Epilepsy
126894871 12689487 2 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
126894871 12689487 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126894871 12689487 Dehydration
126894871 12689487 Exposure during breast feeding
126894871 12689487 Foetal exposure during pregnancy
126894871 12689487 Gastrooesophageal reflux disease
126894871 12689487 Selective eating disorder
126894871 12689487 Urinary tract infection

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

no results found

Therapies reported

no results found