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
112039166 11203916 6 F 201603 20160830 20150619 20160901 EXP US-GLAXOSMITHKLINE-US2015GSK086196 GLAXOSMITHKLINE 58.40 YR F Y 0.00000 20160901 MD 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
112039166 11203916 1 PS LAMICTAL XR LAMOTRIGINE 1 Unknown UNK, U U 22115 200 MG PROLONGED-RELEASE TABLET
112039166 11203916 2 SS NARDIL PHENELZINE SULFATE 1 UNK U 2364004 0
112039166 11203916 3 SS NARDIL PHENELZINE SULFATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112039166 11203916 1 Seizure
112039166 11203916 2 Antidepressant therapy
112039166 11203916 3 Anxiety

Outcome of event

Event ID CASEID OUTC COD
112039166 11203916 HO
112039166 11203916 DS
112039166 11203916 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112039166 11203916 Adverse event
112039166 11203916 Disability
112039166 11203916 Drug dose omission
112039166 11203916 Drug ineffective
112039166 11203916 Hospitalisation
112039166 11203916 Road traffic accident

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
112039166 11203916 1 2007 0
112039166 11203916 2 201603 0