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
115799975 11579997 5 F 2015 20160831 20150930 20160908 EXP US-JAZZ-2015-US-014729 JAZZ 0.00 M Y 0.00000 20160908 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
115799975 11579997 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID U 21196 2.25 G ORAL SOLUTION
115799975 11579997 2 SS XYREM SODIUM OXYBATE 1 Oral DOSE ADJUSTMENTS U 21196 ORAL SOLUTION
115799975 11579997 3 SS XYREM SODIUM OXYBATE 1 Oral 4.5 G, BID U 21196 4.5 G ORAL SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115799975 11579997 1 Narcolepsy
115799975 11579997 2 Cataplexy

Outcome of event

Event ID CASEID OUTC COD
115799975 11579997 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115799975 11579997 Blood cholesterol abnormal
115799975 11579997 Blood pressure abnormal
115799975 11579997 Depression
115799975 11579997 Diabetes mellitus
115799975 11579997 Glycosylated haemoglobin increased
115799975 11579997 Intentional product use issue
115799975 11579997 Osteoarthritis
115799975 11579997 Post-traumatic stress disorder
115799975 11579997 Weight decreased

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
115799975 11579997 1 200312 2003 0
115799975 11579997 3 201009 0