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
91406465 9140646 5 F 20130203 20160906 20130305 20160907 EXP US-GLAXOSMITHKLINE-A1011459A GLAXOSMITHKLINE 29.77 YR F Y 0.00000 20160907 OT 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
91406465 9140646 1 PS LAMICTAL LAMOTRIGINE 1 Unknown 200 MG UNKNOWN DOSING Y U 20241 200 MG TABLET
91406465 9140646 2 SS LAMICTAL LAMOTRIGINE 1 UNK Y U UNKNOWN 20241 TABLET
91406465 9140646 3 SS LAMOTRIGINE. LAMOTRIGINE 1 200 MG, UNK U 20241 200 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
91406465 9140646 1 Seizure
91406465 9140646 3 Seizure

Outcome of event

Event ID CASEID OUTC COD
91406465 9140646 OT
91406465 9140646 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
91406465 9140646 Acne
91406465 9140646 Aura
91406465 9140646 Disorientation
91406465 9140646 Drug dose omission
91406465 9140646 Headache
91406465 9140646 Hypersensitivity
91406465 9140646 Loss of consciousness
91406465 9140646 Rash
91406465 9140646 Seizure
91406465 9140646 Somnolence

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
91406465 9140646 1 20090127 0
91406465 9140646 3 2015 0