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
126923883 12692388 3 F 2016 20160920 20160828 20160926 PER US-SHIRE-US201610550 SHIRE 30.88 YR F Y 56.69000 KG 20160926 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
126923883 12692388 1 PS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 50 MG, 1X/DAY:QD AF1836C 21977 50 MG CAPSULE QD
126923883 12692388 2 SS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 70 MG, UNKNOWN 21977 70 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126923883 12692388 1 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126923883 12692388 Drug ineffective
126923883 12692388 Energy increased
126923883 12692388 Feeling abnormal
126923883 12692388 Lethargy
126923883 12692388 Mental disorder
126923883 12692388 Product quality issue
126923883 12692388 Sleep disorder
126923883 12692388 Urine amphetamine negative

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
126923883 12692388 1 2014 0