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
127687181 12768718 1 I 20160531 20160921 20160921 PER US-JAZZ-2016-US-010087 JAZZ 0.00 F Y 0.00000 20160921 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
127687181 12768718 1 PS XYREM SODIUM OXYBATE 1 Oral 4.5 G, BID U 21196 4.5 G ORAL SOLUTION
127687181 12768718 2 SS XYREM SODIUM OXYBATE 1 Oral 4.5 G, BID U 21196 4.5 G ORAL SOLUTION
127687181 12768718 3 SS XYREM SODIUM OXYBATE 1 Oral DOSE ADJUSTMENT U 21196 ORAL SOLUTION
127687181 12768718 4 SS XYREM SODIUM OXYBATE 1 Oral 3 G, BID U 21196 3 G ORAL SOLUTION
127687181 12768718 5 SS NUVIGIL ARMODAFINIL 1 250 MG 0 TABLET
127687181 12768718 6 C AMBIEN ZOLPIDEM TARTRATE 1 U 0
127687181 12768718 7 C IMITREX SUMATRIPTAN SUCCINATE 1 U 0
127687181 12768718 8 C PROVIGIL MODAFINIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127687181 12768718 1 Narcolepsy
127687181 12768718 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127687181 12768718 Feeling jittery

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
127687181 12768718 1 200809 2009 0
127687181 12768718 2 200909 200911 0
127687181 12768718 3 200911 201302 0
127687181 12768718 4 201302 0
127687181 12768718 5 20160331 0