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
106987752 10698775 2 F 2009 20160919 20150108 20160921 PER US-GLAXOSMITHKLINE-US2014GSK045860 GLAXOSMITHKLINE 0.00 M Y 0.00000 20160921 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
106987752 10698775 1 PS LAMICTAL LAMOTRIGINE 1 Unknown 200 MG, U U UNKNOWN 20241 200 MG TABLET
106987752 10698775 2 SS LAMICTAL XR LAMOTRIGINE 1 Unknown 50 MG, U U UNKNOWN 0 50 MG PROLONGED-RELEASE TABLET
106987752 10698775 3 SS Lamotrigine Prolonged-release tablet LAMOTRIGINE 1 Unknown UNK, U U UNKNOWN 0 PROLONGED-RELEASE TABLET
106987752 10698775 4 SS Lamotrigine Tablet LAMOTRIGINE 1 200 MG, BID Y UNKNOWN 20241 200 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106987752 10698775 1 Product used for unknown indication
106987752 10698775 2 Product used for unknown indication
106987752 10698775 3 Product used for unknown indication
106987752 10698775 4 Seizure

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
106987752 10698775 Asthenia
106987752 10698775 Diarrhoea
106987752 10698775 Feeling abnormal
106987752 10698775 Headache
106987752 10698775 Impaired work ability
106987752 10698775 Malaise
106987752 10698775 Vomiting

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
106987752 10698775 4 2009 0