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
125717391 12571739 1 I 2016 20160717 20160719 20160719 PER US-SHIRE-US201608946 SHIRE 23.09 YR F Y 0.00000 20160719 PH 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
125717391 12571739 1 PS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 40 MG, 1X/DAY:QD 21977 40 MG CAPSULE QD
125717391 12571739 2 SS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 50 MG, 1X/DAY:QD 21977 50 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125717391 12571739 1 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125717391 12571739 Disturbance in attention
125717391 12571739 Drug effect decreased
125717391 12571739 Drug ineffective
125717391 12571739 Performance status decreased
125717391 12571739 Product quality issue

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
125717391 12571739 1 201511 201606 0
125717391 12571739 2 201606 0