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
127225981 12722598 1 I 2012 20160826 20160907 20160907 PER US-SHIRE-US201611455 SHIRE 0.00 M Y 90.70000 KG 20160907 MD 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
127225981 12722598 1 PS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 20 MG, 1X/DAY:QD 21977 20 MG CAPSULE QD
127225981 12722598 2 SS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 40 MG, 2X/DAY:BID 21977 40 MG CAPSULE BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127225981 12722598 1 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127225981 12722598 Drug effect variable
127225981 12722598 Fluid retention
127225981 12722598 Hunger
127225981 12722598 Inappropriate schedule of drug administration
127225981 12722598 Prescribed overdose
127225981 12722598 Product quality issue
127225981 12722598 Weight increased

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
127225981 12722598 1 2012 0