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
127477621 12747762 1 I 20160525 20160525 20160915 20160915 PER US-JAZZ-2016-US-010026 JAZZ 17.07 YR F Y 0.00000 20160915 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
127477621 12747762 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
127477621 12747762 2 SS XYREM SODIUM OXYBATE 1 21196 ORAL SOLUTION
127477621 12747762 3 SS TOPAMAX TOPIRAMATE 1 U 0
127477621 12747762 4 C Gildess Fe ETHINYL ESTRADIOLNORETHINDRONE 1 U 0
127477621 12747762 5 C LEVOTHYROXINE. LEVOTHYROXINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127477621 12747762 1 Narcolepsy
127477621 12747762 2 Cataplexy
127477621 12747762 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127477621 12747762 Constipation
127477621 12747762 Fatigue
127477621 12747762 Headache
127477621 12747762 Paraesthesia

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
127477621 12747762 1 20160524 0