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
127167151 12716715 1 I 20160829 20160906 20160906 EXP US-JAZZ-2016-US-016583 JAZZ 0.00 M Y 0.00000 20160906 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
127167151 12716715 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID U 21196 2.25 G ORAL SOLUTION
127167151 12716715 2 SS Oxycodone OXYCODONE 1 0
127167151 12716715 3 SS NUVIGIL ARMODAFINIL 1 250 MG TABLET, BREAKING THE TABLET INTO HALF AND TAKING HALF A TABLET TWICE DAILY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127167151 12716715 1 Narcolepsy
127167151 12716715 2 Product used for unknown indication
127167151 12716715 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127167151 12716715 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127167151 12716715 Tonsillectomy
127167151 12716715 Unevaluable event
127167151 12716715 Withdrawal syndrome

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
127167151 12716715 1 201505 2015 0