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
126043101 12604310 1 I 201601 20160211 20160728 20160728 PER US-JAZZ-2016-US-002684 JAZZ 42.15 YR F Y 0.00000 20160728 CN 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
126043101 12604310 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
126043101 12604310 2 SS XYREM SODIUM OXYBATE 1 21196 ORAL SOLUTION
126043101 12604310 3 SS PROVIGIL MODAFINIL 1 UNK 0 TABLET
126043101 12604310 4 C PROAIR HFA ALBUTEROL SULFATE 1 UNK U 0 INHALER
126043101 12604310 5 C ATIVAN LORAZEPAM 1 UNK U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126043101 12604310 1 Narcolepsy
126043101 12604310 2 Cataplexy
126043101 12604310 3 Product used for unknown indication
126043101 12604310 4 Product used for unknown indication
126043101 12604310 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126043101 12604310 Drug ineffective
126043101 12604310 Unevaluable event

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
126043101 12604310 1 201601 0
126043101 12604310 3 20151222 0
126043101 12604310 4 20160121 0
126043101 12604310 5 20151222 0