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
109950462 10995046 2 F 20160712 20150407 20160722 EXP US-GLAXOSMITHKLINE-US2015GSK022738 GLAXOSMITHKLINE 0.00 M Y 0.00000 20160722 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
109950462 10995046 1 PS LAMICTAL XR LAMOTRIGINE 1 Unknown 100 MG, TID 22115 100 MG PROLONGED-RELEASE TABLET TID
109950462 10995046 2 SS LAMICTAL XR LAMOTRIGINE 1 Unknown UNK, VA 22115 PROLONGED-RELEASE TABLET
109950462 10995046 3 SS LAMOTRIGINE. LAMOTRIGINE 1 Unknown UNK, U U 0
109950462 10995046 4 SS Lamotrigine Prolonged-release tablet LAMOTRIGINE 1 UNK, U 22115 PROLONGED-RELEASE TABLET
109950462 10995046 5 C DEPAKOTE DIVALPROEX SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109950462 10995046 1 Complex partial seizures
109950462 10995046 3 Epilepsy
109950462 10995046 4 Complex partial seizures
109950462 10995046 5 Complex partial seizures

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
109950462 10995046 Drug ineffective
109950462 10995046 Inability to afford medication
109950462 10995046 Intentional underdose
109950462 10995046 Product substitution issue

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

no results found

Therapies reported

no results found