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
124974262 12497426 2 F 20160922 20160624 20160930 EXP US-JAZZ-2016-US-011307 JAZZ 0.00 F Y 0.00000 20160930 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
124974262 12497426 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID U 21196 2.25 G ORAL SOLUTION
124974262 12497426 2 SS XYREM SODIUM OXYBATE 1 Oral 3 G, BID U 21196 3 G ORAL SOLUTION
124974262 12497426 3 SS XYREM SODIUM OXYBATE 1 Oral 3 G, BID U 21196 3 G ORAL SOLUTION
124974262 12497426 4 C PROVIGIL MODAFINIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124974262 12497426 1 Apnoea
124974262 12497426 2 Hypersomnia
124974262 12497426 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124974262 12497426 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124974262 12497426 Expired product administered
124974262 12497426 Intentional product misuse
124974262 12497426 Malaise
124974262 12497426 Surgery

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
124974262 12497426 1 200704 200708 0
124974262 12497426 2 200708 0
124974262 12497426 3 201606 0