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
127779081 12777908 1 I 201601 20160609 20160924 20160924 PER US-JAZZ-2016-US-010824 JAZZ 35.07 YR M Y 0.00000 20160924 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
127779081 12777908 1 PS XYREM SODIUM OXYBATE 1 Oral 3 G, BID 21196 3 G ORAL SOLUTION
127779081 12777908 2 SS XYREM SODIUM OXYBATE 1 Oral DOSE ADJUSTMENTS 21196 ORAL SOLUTION
127779081 12777908 3 SS XYREM SODIUM OXYBATE 1 Oral 4.5 G, BID 21196 4.5 G ORAL SOLUTION
127779081 12777908 4 SS AMBIEN ZOLPIDEM TARTRATE 1 UNK N 0 TABLET
127779081 12777908 5 C ERYTHROMYCIN ESTOLATE. ERYTHROMYCIN ESTOLATE 1 U 0
127779081 12777908 6 C IBUPROFEN. IBUPROFEN 1 U 0
127779081 12777908 7 C NUVIGIL ARMODAFINIL 1 U 0
127779081 12777908 8 C LUNESTA ESZOPICLONE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127779081 12777908 1 Narcolepsy
127779081 12777908 2 Cataplexy
127779081 12777908 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127779081 12777908 Amnesia
127779081 12777908 Arthralgia
127779081 12777908 Cerebral disorder
127779081 12777908 Weight decreased

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
127779081 12777908 1 200903 200903 0
127779081 12777908 2 200903 201605 0
127779081 12777908 3 201605 0
127779081 12777908 4 20151222 20160531 0