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
124512463 12451246 3 F 2014 20160818 20160609 20160824 EXP US-NOVEN PHARMACEUTICALS, INC.-US2016001377 NOVEN 0.00 Y 0.00000 20160824 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
124512463 12451246 1 PS DAYTRANA METHYLPHENIDATE 1 Transdermal 30 MG, UNKNOWN Y UNK 21514 30 MG TRANSDERMAL PATCH
124512463 12451246 2 SS DAYTRANA METHYLPHENIDATE 1 Transdermal USING ONE 10MG AND ONE 20MG PATCH AT A TIME, UNKNOWN Y 79227 21514 30 MG TRANSDERMAL PATCH

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124512463 12451246 1 Attention deficit/hyperactivity disorder

Outcome of event

Event ID CASEID OUTC COD
124512463 12451246 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124512463 12451246 Application site ulcer
124512463 12451246 Drug administered at inappropriate site
124512463 12451246 Emotional disorder
124512463 12451246 Impulsive behaviour
124512463 12451246 Off label use
124512463 12451246 Product quality issue
124512463 12451246 Verbal abuse
124512463 12451246 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
124512463 12451246 1 2014 201605 0
124512463 12451246 2 201605 201607 0