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
126813172 12681317 2 F 20160704 20160829 20160824 20160907 EXP US-SA-2016SA149869 AVENTIS 57.00 YR A F Y 0.00000 20160907 OT 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
126813172 12681317 1 PS AMBIEN ZOLPIDEM TARTRATE 1 Unknown U UNKNOWN 19908
126813172 12681317 2 SS XANAX ALPRAZOLAM 1 Unknown U UNKNOWN 0
126813172 12681317 3 SS SOMA CARISOPRODOL 1 Oral Y UNKNOWN 0
126813172 12681317 4 SS ATIVAN LORAZEPAM 1 Oral Y UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126813172 12681317 3 Myalgia

Outcome of event

Event ID CASEID OUTC COD
126813172 12681317 OT
126813172 12681317 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126813172 12681317 Abasia
126813172 12681317 Coma
126813172 12681317 Dysphagia
126813172 12681317 Hypotonia

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
126813172 12681317 3 20160704 0
126813172 12681317 4 20160704 0