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
126190192 12619019 2 F 201607 20160729 20160803 20160818 PER US-SHIRE-US201608845 SHIRE 31.33 YR M Y 65.76000 KG 20160818 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
126190192 12619019 1 PS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 40 MG, 1X/DAY:QD 3139733 21977 40 MG CAPSULE QD
126190192 12619019 2 SS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 10 MG, 1X/DAY:QD 21977 10 MG CAPSULE QD
126190192 12619019 3 SS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 20 MG, 1X/DAY:QD 21977 20 MG CAPSULE QD
126190192 12619019 4 SS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 30 MG, 1X/DAY:QD 21977 30 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126190192 12619019 1 Binge eating

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126190192 12619019 Binge eating
126190192 12619019 Condition aggravated
126190192 12619019 Drug effect decreased
126190192 12619019 Hypermetabolism
126190192 12619019 Product quality issue
126190192 12619019 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
126190192 12619019 1 201606 0
126190192 12619019 2 201603 201604 0
126190192 12619019 3 201604 201606 0
126190192 12619019 4 201606 201606 0