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
126868772 12686877 2 F 20160411 20160825 20160912 PER US-JAZZ-2016-US-006881 JAZZ 0.00 F Y 0.00000 20160912 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
126868772 12686877 1 PS XYREM SODIUM OXYBATE 1 Oral 3 G, BID 21196 3 G ORAL SOLUTION
126868772 12686877 2 SS XYREM SODIUM OXYBATE 1 Oral DOSE ADJUSTMENTS 21196 ORAL SOLUTION
126868772 12686877 3 SS XYREM SODIUM OXYBATE 1 Oral 3 G, TID 21196 3 G ORAL SOLUTION
126868772 12686877 4 SS PROVIGIL MODAFINIL 1 U 0
126868772 12686877 5 C QUETIAPINE FUMARATE. QUETIAPINE FUMARATE 1 U 0
126868772 12686877 6 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 U 0
126868772 12686877 7 C SEROQUEL QUETIAPINE FUMARATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126868772 12686877 1 Narcolepsy
126868772 12686877 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126868772 12686877 Depression

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
126868772 12686877 1 200804 200811 0
126868772 12686877 3 201407 0