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
126463871 12646387 1 I 201604 20160531 20160812 20160812 EXP US-NOVEN PHARMACEUTICALS, INC.-US2016001274 NOVEN 0.00 Y 0.00000 20160812 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
126463871 12646387 1 PS DAYTRANA METHYLPHENIDATE 1 Transdermal 30 MG, UNKNOWN UNK 21514 30 MG TRANSDERMAL PATCH
126463871 12646387 2 SS DAYTRANA METHYLPHENIDATE 1 Transdermal 30 MG, UNKNOWN UNK 21514 30 MG TRANSDERMAL PATCH
126463871 12646387 3 SS METHYLPHENIDATE HYDROCHLORIDE. METHYLPHENIDATE HYDROCHLORIDE 1 Oral 60 ML, UNKNOWN Y UNK 0 60 ML
126463871 12646387 4 SS Fluoxetine Hcl FLUOXETINE HYDROCHLORIDE 1 Oral UNK, UNKNOWN Y UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126463871 12646387 1 Attention deficit/hyperactivity disorder
126463871 12646387 3 Attention deficit/hyperactivity disorder
126463871 12646387 4 Attention deficit/hyperactivity disorder

Outcome of event

Event ID CASEID OUTC COD
126463871 12646387 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126463871 12646387 Drug dose omission
126463871 12646387 Surgery

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
126463871 12646387 1 2012 201604 0
126463871 12646387 2 2016 0