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
127686611 12768661 1 I 201605 20160531 20160921 20160921 PER US-JAZZ-2016-US-010152 JAZZ 23.55 YR F Y 0.00000 20160921 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
127686611 12768661 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
127686611 12768661 2 SS XYREM SODIUM OXYBATE 1 Oral 3 G, BID 21196 3 G ORAL SOLUTION
127686611 12768661 3 SS RITALIN METHYLPHENIDATE HYDROCHLORIDE 1 UNK 0
127686611 12768661 4 C ABILIFY ARIPIPRAZOLE 1 U 0
127686611 12768661 5 C IBUPROFEN. IBUPROFEN 1 U 0
127686611 12768661 6 C IMITREX SUMATRIPTAN SUCCINATE 1 U 0
127686611 12768661 7 C LITHIUM CARBONATE. LITHIUM CARBONATE 1 U 0
127686611 12768661 8 C PROAIR HFA ALBUTEROL SULFATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127686611 12768661 1 Narcolepsy
127686611 12768661 2 Cataplexy
127686611 12768661 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127686611 12768661 Anxiety
127686611 12768661 Asthma
127686611 12768661 Depression

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
127686611 12768661 1 201605 201605 0
127686611 12768661 2 201605 0