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
125239641 12523964 1 I 20151225 20160704 20160704 PER US-JAZZ-2015-US-022523 JAZZ 0.00 M Y 0.00000 20160704 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
125239641 12523964 1 PS XYREM SODIUM OXYBATE 1 Oral 3 G, FIRST DOSE 21196 3 G ORAL SOLUTION
125239641 12523964 2 SS XYREM SODIUM OXYBATE 1 Oral 5 G, SECOND DOSE 21196 5 G ORAL SOLUTION
125239641 12523964 3 SS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
125239641 12523964 4 SS ZANAFLEX TIZANIDINE HYDROCHLORIDE 1 6 MG, FIRST DOSE U 0 6 MG
125239641 12523964 5 SS ZANAFLEX TIZANIDINE HYDROCHLORIDE 1 4 MG, SECOND DOSE U 0 4 MG
125239641 12523964 6 C BACLOFEN. BACLOFEN 1 UNK U 0
125239641 12523964 7 C KLONOPIN CLONAZEPAM 1 UNK U 0
125239641 12523964 8 C LIBRIUM CHLORDIAZEPOXIDE HYDROCHLORIDE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125239641 12523964 1 Narcolepsy
125239641 12523964 4 Product used for unknown indication
125239641 12523964 6 Product used for unknown indication
125239641 12523964 7 Product used for unknown indication
125239641 12523964 8 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125239641 12523964 Intentional product use issue
125239641 12523964 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
125239641 12523964 1 200809 2008 0
125239641 12523964 2 200809 2008 0
125239641 12523964 3 201211 0