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
125705411 12570541 1 I 2016 20160623 20160719 20160719 PER US-SHIRE-US201607980 SHIRE 42.00 YR M Y 72.56000 KG 20160719 OT 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
125705411 12570541 1 PS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 40 MG, 2X/DAY:BID (ONCE IN TEH MORNING AND ONCE IN THE AFTERNOON) 21977 40 MG CAPSULE BID
125705411 12570541 2 C LATUDA LURASIDONE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN 0
125705411 12570541 3 C LITHIUM. LITHIUM 1 Unknown UNK, UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125705411 12570541 1 Attention deficit/hyperactivity disorder
125705411 12570541 2 Product used for unknown indication
125705411 12570541 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125705411 12570541 Drug effect decreased
125705411 12570541 Inappropriate schedule of drug administration
125705411 12570541 Prescribed overdose

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
125705411 12570541 1 2016 0