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
124209953 12420995 3 F 201605 20160720 20160531 20160722 EXP US-GLAXOSMITHKLINE-US2016GSK077208 GLAXOSMITHKLINE 46.56 YR F 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
124209953 12420995 1 PS LAMICTAL XR LAMOTRIGINE 1 300 MG, U U 22115 300 MG PROLONGED-RELEASE TABLET
124209953 12420995 2 SS LEVETIRACETAM. LEVETIRACETAM 1 UNK, U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124209953 12420995 1 Generalised tonic-clonic seizure
124209953 12420995 2 Seizure

Outcome of event

Event ID CASEID OUTC COD
124209953 12420995 OT
124209953 12420995 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124209953 12420995 Adverse drug reaction
124209953 12420995 Disorientation
124209953 12420995 Dizziness
124209953 12420995 Drug dose omission
124209953 12420995 Drug ineffective
124209953 12420995 Hospitalisation
124209953 12420995 Hunger
124209953 12420995 Seizure
124209953 12420995 Suture insertion

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
124209953 12420995 1 2014 0
124209953 12420995 2 20160522 0