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
125305971 12530597 1 I 20160620 20160706 20160706 EXP US-GLAXOSMITHKLINE-US2016GSK088866 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160706 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
125305971 12530597 1 PS LAMICTAL LAMOTRIGINE 1 100 MG, U U 011001305 20241 100 MG TABLET
125305971 12530597 2 SS LAMICTAL LAMOTRIGINE 1 U 20241 TABLET
125305971 12530597 3 SS LAMOTRIGINE. LAMOTRIGINE 1 UNK, U 20241
125305971 12530597 4 SS LAMOTRIGINE. LAMOTRIGINE 1 20241
125305971 12530597 5 SS ZONISAMIDE. ZONISAMIDE 1 200 MG, U U UNKNOWN 0 200 MG
125305971 12530597 6 SS ZONISAMIDE. ZONISAMIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125305971 12530597 1 Epilepsy
125305971 12530597 2 Seizure
125305971 12530597 3 Seizure
125305971 12530597 4 Epilepsy
125305971 12530597 5 Epilepsy
125305971 12530597 6 Seizure

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125305971 12530597 Dizziness
125305971 12530597 Drug ineffective
125305971 12530597 Feeling abnormal
125305971 12530597 Product substitution issue

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
125305971 12530597 1 1999 0
125305971 12530597 3 2000 0
125305971 12530597 5 2013 0