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
116897404 11689740 4 F 20160823 20151102 20160830 EXP JP-GLAXOSMITHKLINE-JP2015JPN152159 GLAXOSMITHKLINE 43.00 YR F Y 0.00000 20160830 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
116897404 11689740 1 PS LAMICTAL LAMOTRIGINE 1 Oral UNK 20241 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116897404 11689740 1 Bipolar disorder

Outcome of event

Event ID CASEID OUTC COD
116897404 11689740 OT
116897404 11689740 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
116897404 11689740 Aphthous ulcer
116897404 11689740 Cough
116897404 11689740 Drug eruption
116897404 11689740 Drug reaction with eosinophilia and systemic symptoms
116897404 11689740 Enanthema
116897404 11689740 Generalised erythema
116897404 11689740 Hepatic function abnormal
116897404 11689740 Lymphadenopathy
116897404 11689740 Neutrophil count increased
116897404 11689740 Oropharyngeal pain
116897404 11689740 Pyrexia
116897404 11689740 Rash
116897404 11689740 Swelling face
116897404 11689740 White blood cell count increased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found