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
125239011 12523901 1 I 20151222 20160704 20160704 PER US-JAZZ-2015-US-022306 JAZZ 0.00 F Y 0.00000 20160704 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
125239011 12523901 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID U 21196 2.25 G ORAL SOLUTION
125239011 12523901 2 SS XYREM SODIUM OXYBATE 1 Oral 3 G, BID U 21196 3 G ORAL SOLUTION
125239011 12523901 3 SS XYREM SODIUM OXYBATE 1 Oral 6.5 G, BID U 21196 6.5 G ORAL SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125239011 12523901 1 Narcolepsy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125239011 12523901 Abnormal sleep-related event
125239011 12523901 Fall
125239011 12523901 Fatigue
125239011 12523901 Memory impairment
125239011 12523901 Snoring

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
125239011 12523901 1 200502 2005 0
125239011 12523901 2 2005 200505 0
125239011 12523901 3 200505 0