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
124883034 12488303 4 F 20160927 20160622 20160930 PER US-GLAXOSMITHKLINE-US2016GSK082140 GLAXOSMITHKLINE 0.00 M Y 0.00000 20160930 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
124883034 12488303 1 PS COREG CARVEDILOL 1 U 20297 TABLET
124883034 12488303 2 SS Lamotrigine Tablet LAMOTRIGINE 1 200 MG, UNK U UNKNOWN 0 200 MG TABLET
124883034 12488303 3 SS Lamotrigine Tablet LAMOTRIGINE 1 25 MG, UNK U UNKNOWN 0 25 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124883034 12488303 1 Cardiac disorder
124883034 12488303 2 Bipolar disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124883034 12488303 Disturbance in attention
124883034 12488303 Drug intolerance
124883034 12488303 Ill-defined disorder
124883034 12488303 Malaise
124883034 12488303 Memory impairment

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
124883034 12488303 2 20070310 0