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
126409401 12640940 1 I 201605 20160527 20160810 20160810 EXP JP-GLAXOSMITHKLINE-JP2016JPN076087 GLAXOSMITHKLINE 16.55 YR F Y 50.00000 KG 20160810 CN JP JP

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
126409401 12640940 1 PS LAMICTAL LAMOTRIGINE 1 Oral 25 MG, QOD Y 20241 25 MG TABLET QOD
126409401 12640940 2 C DEPAKENE VALPROIC ACID 1 400 MG, 1D 0 400 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126409401 12640940 1 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
126409401 12640940 HO
126409401 12640940 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126409401 12640940 Ascites
126409401 12640940 Aspiration
126409401 12640940 Computerised tomogram thorax abnormal
126409401 12640940 Confusional state
126409401 12640940 Decreased appetite
126409401 12640940 Drug eruption
126409401 12640940 Hepatic function abnormal
126409401 12640940 Platelet count decreased
126409401 12640940 Pleural effusion
126409401 12640940 Pneumonia
126409401 12640940 Pyrexia
126409401 12640940 Rash erythematous

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
126409401 12640940 1 20160506 20160519 0