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
127446151 12744615 1 I 201605 20160516 20160914 20160914 PER US-JAZZ-2016-US-009185 JAZZ 27.49 YR F Y 0.00000 20160914 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
127446151 12744615 1 PS XYREM SODIUM OXYBATE 1 Oral 2 G, BID 21196 2 G ORAL SOLUTION
127446151 12744615 2 SS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
127446151 12744615 3 SS XANAX ALPRAZOLAM 1 UNK N 0
127446151 12744615 4 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 U 0
127446151 12744615 5 C ALPRAZOLAM ER ALPRAZOLAM 1 U 0
127446151 12744615 6 C L-methylfolate forte 2 U 0
127446151 12744615 7 C LO LOESTRIN FE ETHINYL ESTRADIOLNORETHINDRONE ACETATE 1 U 0
127446151 12744615 8 C PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 U 0
127446151 12744615 9 C Propranolol er 2 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127446151 12744615 1 Narcolepsy
127446151 12744615 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127446151 12744615 Anxiety
127446151 12744615 Confusional state
127446151 12744615 Drug withdrawal syndrome

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
127446151 12744615 1 201605 201605 0
127446151 12744615 2 201605 0
127446151 12744615 3 201605 0