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
127762521 12776252 1 I 20160906 20160914 20160923 20160923 PER US-SHIRE-US201612601 SHIRE 12.00 YR M Y 51.70000 KG 20160923 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
127762521 12776252 1 PS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 50 MG, 1X/DAY:QD 150 MG Y 21977 50 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127762521 12776252 1 Attention deficit/hyperactivity disorder

Outcome of event

Event ID CASEID OUTC COD
127762521 12776252 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127762521 12776252 Adverse event
127762521 12776252 Chest discomfort
127762521 12776252 Dry mouth
127762521 12776252 Dyspnoea
127762521 12776252 Feeling abnormal
127762521 12776252 Heart rate increased
127762521 12776252 Hypersensitivity
127762521 12776252 Hypoaesthesia
127762521 12776252 Muscle contracture
127762521 12776252 Paraesthesia
127762521 12776252 Respiratory rate increased
127762521 12776252 Thirst

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
127762521 12776252 1 20160906 20160908 0