The Safety Rates Drug Report

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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
125239151 12523915 1 I 20151222 20160704 20160704 PER US-JAZZ-2015-US-022332 JAZZ 0.00 M 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
125239151 12523915 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
125239151 12523915 2 SS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
125239151 12523915 3 SS XYREM SODIUM OXYBATE 1 Oral DOSE ADJUSTMENTS 21196 ORAL SOLUTION
125239151 12523915 4 SS XYREM SODIUM OXYBATE 1 Oral 4.5 G, BID 21196 4.5 G ORAL SOLUTION
125239151 12523915 5 C Methadone hcl METHADONE HYDROCHLORIDE 1 UNK U 0 POWDER
125239151 12523915 6 C DESOXYN METHAMPHETAMINE HYDROCHLORIDE 1 UNK U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125239151 12523915 1 Narcolepsy
125239151 12523915 2 Cataplexy
125239151 12523915 5 Product used for unknown indication
125239151 12523915 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125239151 12523915 Condition aggravated
125239151 12523915 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
125239151 12523915 1 200702 2007 0
125239151 12523915 2 2013 2013 0
125239151 12523915 4 201311 0
125239151 12523915 5 20131220 0
125239151 12523915 6 20100501 0