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
126683141 12668314 1 I 2013 20160810 20160819 20160819 PER US-SHIRE-US201610433 SHIRE 0.00 F Y 77.98000 KG 20160819 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
126683141 12668314 1 PS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 30 MG, 1X/DAY:QD 21977 30 MG CAPSULE QD
126683141 12668314 2 SS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 40 MG, 1X/DAY:QD 21977 40 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126683141 12668314 1 Attention deficit/hyperactivity disorder
126683141 12668314 2 Binge eating

Outcome of event

Event ID CASEID OUTC COD
126683141 12668314 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126683141 12668314 Asthenia
126683141 12668314 Disturbance in attention
126683141 12668314 Drug effect decreased
126683141 12668314 Drug effect incomplete
126683141 12668314 Drug effect variable
126683141 12668314 Drug ineffective
126683141 12668314 Drug tolerance
126683141 12668314 Somnolence
126683141 12668314 Weight decreased

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
126683141 12668314 1 2013 2015 0
126683141 12668314 2 2015 0