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
125379801 12537980 1 I 20160119 20160627 20160707 20160707 EXP FR-SA-2016SA120176 AVENTIS 26.00 YR A F Y 0.00000 20160707 OT FR FR

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
125379801 12537980 1 SS PARACETAMOL ACETAMINOPHEN 1 Oral INTAKE BETWEEN 00:00 AND 1:00 IN THE MORNING UNKNOWN 0 48 G 1X
125379801 12537980 2 SS IBUPROFEN. IBUPROFEN 1 Oral UNKNOWN 0 4800 MG TABLET 1X
125379801 12537980 3 PS STILNOX ZOLPIDEM TARTRATE 1 Oral UNKNOWN 19908 340 MG TABLET 1X
125379801 12537980 4 SS ZOPICLONE ZOPICLONE 1 Oral UNKNOWN 0 14 DF TABLET 1X
125379801 12537980 5 SS ALPRAZOLAM. ALPRAZOLAM 1 Oral UNKNOWN 0 14 DF TABLET 1X

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125379801 12537980 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125379801 12537980 Acute hepatic failure
125379801 12537980 Somnolence

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
125379801 12537980 1 20160119 20160119 0
125379801 12537980 2 20160119 20160119 0
125379801 12537980 3 20160119 20160119 0
125379801 12537980 4 20160119 20160119 0
125379801 12537980 5 20160119 20160119 0