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
126903912 12690391 2 F 2016 20160913 20160826 20160921 EXP US-SHIRE-US201610499 SHIRE 48.33 YR M Y 0.00000 20160921 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
126903912 12690391 1 PS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 70 MG, 1X/DAY:QD D 21977 70 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126903912 12690391 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126903912 12690391 HO
126903912 12690391 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126903912 12690391 Asthenia
126903912 12690391 Chest discomfort
126903912 12690391 Chest pain
126903912 12690391 Chills
126903912 12690391 Drug dose omission
126903912 12690391 Drug withdrawal syndrome
126903912 12690391 Feeling abnormal
126903912 12690391 Pain
126903912 12690391 Pyrexia
126903912 12690391 Tachycardia
126903912 12690391 Tremor

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
126903912 12690391 1 2005 0