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
126708911 12670891 1 I 20160401 20160822 20160822 PER US-JAZZ-2016-US-006325 JAZZ 0.00 M Y 0.00000 20160822 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
126708911 12670891 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
126708911 12670891 2 SS XYREM SODIUM OXYBATE 1 Oral DOSE ADJUSTMENTS 21196 ORAL SOLUTION
126708911 12670891 3 SS XYREM SODIUM OXYBATE 1 Oral 4.5 G, BID 21196 4.5 G ORAL SOLUTION
126708911 12670891 4 SS NUVIGIL ARMODAFINIL 1 UNK U 0 TABLET
126708911 12670891 5 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126708911 12670891 1 Narcolepsy
126708911 12670891 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126708911 12670891 Disorientation
126708911 12670891 Drug ineffective
126708911 12670891 Hypersensitivity
126708911 12670891 Sluggishness

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
126708911 12670891 1 201601 201601 0
126708911 12670891 2 201601 201601 0
126708911 12670891 3 201601 0
126708911 12670891 4 20160107 0