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
126470201 12647020 1 I 201607 20160726 20160812 20160812 PER US-SHIRE-US201609431 SHIRE 30.95 YR F Y 62.13000 KG 20160812 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
126470201 12647020 1 PS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 40 MG, 1X/DAY:QD 21977 40 MG CAPSULE QD
126470201 12647020 2 C LOESTRIN NOS ETHINYL ESTRADIOLNORETHINDRONE ACETATE 1 Oral 1 DF, 1X/DAY:QD 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126470201 12647020 1 Attention deficit/hyperactivity disorder
126470201 12647020 2 Contraception

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126470201 12647020 Disturbance in attention
126470201 12647020 Drug effect decreased
126470201 12647020 Incorrect dose administered
126470201 12647020 Product quality issue
126470201 12647020 Wrong technique in product usage process

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
126470201 12647020 1 2014 0
126470201 12647020 2 2013 0