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
125439501 12543950 1 I 20160628 20160711 20160711 EXP US-GLAXOSMITHKLINE-US2016094041 GLAXOSMITHKLINE 0.00 Y 0.00000 20160711 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
125439501 12543950 1 PS EXCEDRIN ACETAMINOPHENASPIRINCAFFEINE 1 8 DF, U U UNKNOWN 20802 8 DF
125439501 12543950 2 SS ASPIRIN. ASPIRIN 1 4 DF, U U UNKNOWN 0 4 DF
125439501 12543950 3 SS TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 3 DF, U U UNKNOWN 0 3 DF
125439501 12543950 4 SS XANAX ALPRAZOLAM 1 1 DF, U U UNKNOWN 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125439501 12543950 1 Migraine
125439501 12543950 2 Product used for unknown indication
125439501 12543950 3 Product used for unknown indication
125439501 12543950 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125439501 12543950 Drug ineffective
125439501 12543950 Feeling jittery
125439501 12543950 Intentional product misuse
125439501 12543950 Labelled drug-drug interaction medication error

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
125439501 12543950 1 20160628 0
125439501 12543950 2 20160628 0
125439501 12543950 3 20160628 0
125439501 12543950 4 20160628 0