The Safety Rates Drug Report

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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
127091531 12709153 1 I 20160506 20160901 20160901 PER US-JAZZ-2016-US-008657 JAZZ 0.00 M Y 0.00000 20160901 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
127091531 12709153 1 PS XYREM SODIUM OXYBATE 1 Oral 2.5 G, BID U 21196 2.5 G ORAL SOLUTION
127091531 12709153 2 SS XYREM SODIUM OXYBATE 1 Oral DOSE ADJUSTMENTS U 21196 ORAL SOLUTION
127091531 12709153 3 SS XYREM SODIUM OXYBATE 1 Oral 4 G, BID U 21196 4 G ORAL SOLUTION
127091531 12709153 4 SS NUVIGIL ARMODAFINIL 1 0
127091531 12709153 5 C DEXTROAMPHETAMINE. DEXTROAMPHETAMINE 1 U 0
127091531 12709153 6 C LOSARTAN. LOSARTAN 1 U 0
127091531 12709153 7 C PROVIGIL MODAFINIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127091531 12709153 1 Narcolepsy
127091531 12709153 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127091531 12709153 Drug ineffective
127091531 12709153 Stress
127091531 12709153 Therapeutic response 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
127091531 12709153 1 200711 200801 0
127091531 12709153 3 200810 2010 0