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
114878202 11487820 2 F 201407 20160908 20150909 20160916 PER US-JAZZ-2015-US-001050 JAZZ 33.89 YR F Y 77.60000 KG 20160916 OT 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
114878202 11487820 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
114878202 11487820 2 SS XYREM SODIUM OXYBATE 1 Oral DOSE ADJUSTMENTS 21196 ORAL SOLUTION
114878202 11487820 3 SS XYREM SODIUM OXYBATE 1 Oral 4.5 G, BID 21196 4.5 G ORAL SOLUTION
114878202 11487820 4 C LASIX FUROSEMIDE 1 20 MG, UNK U 0 20 MG TABLET
114878202 11487820 5 C VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 75 MG, UNK U 0 75 MG SLOW RELEASE CAPSULES
114878202 11487820 6 C ALPRAZOLAM. ALPRAZOLAM 1 0.25 MG, UNK U 0 .25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114878202 11487820 1 Narcolepsy
114878202 11487820 4 Product used for unknown indication
114878202 11487820 5 Product used for unknown indication
114878202 11487820 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
114878202 11487820 Amnesia
114878202 11487820 Anxiety
114878202 11487820 Cognitive disorder

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
114878202 11487820 1 201304 201304 0
114878202 11487820 2 201304 201409 0
114878202 11487820 3 201409 0
114878202 11487820 4 20150112 0
114878202 11487820 5 20150121 0
114878202 11487820 6 20150121 0