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
127832551 12783255 1 I 20160926 0 20160927 20160927 DIR US-FDA-351615 FDA-CTU 30.00 YR M N 128.25000 KG 20160927 Y 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
127832551 12783255 1 PS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral Y Y 0 1 G
127832551 12783255 2 C FISH OIL FISH OIL 1 0
127832551 12783255 4 C MULTI 2 0
127832551 12783255 6 C VITAMIN D3 CHOLECALCIFEROL 1 0
127832551 12783255 8 C MAGNESIUM MAGNESIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127832551 12783255 1 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127832551 12783255 Amnesia
127832551 12783255 Aphasia
127832551 12783255 Confusional state
127832551 12783255 Feeling abnormal
127832551 12783255 Incoherent

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
127832551 12783255 1 20160919 20160926 0