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
124936752 12493675 2 F 201604 20160706 20160623 20160711 EXP CN-GLAXOSMITHKLINE-CN2016GSK089308 GLAXOSMITHKLINE 70.00 YR F Y 0.00000 20160711 CN CN CN

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
124936752 12493675 1 PS LAMICTAL LAMOTRIGINE 1 Oral UNK Y 20241 25 MG TABLET QD
124936752 12493675 2 SS LAMICTAL LAMOTRIGINE 1 25 MG, QD Y 20241 25 MG TABLET QD
124936752 12493675 3 SS OXCARBAZEPINE. OXCARBAZEPINE 1 UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124936752 12493675 1 Epilepsy
124936752 12493675 3 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
124936752 12493675 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124936752 12493675 Drug administration error
124936752 12493675 Nasopharyngitis
124936752 12493675 Pyrexia
124936752 12493675 Rash generalised
124936752 12493675 Wrong technique in product usage process

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
124936752 12493675 1 201604 201604 0