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
126940441 12694044 1 I 20160705 20160829 20160829 PER US-JNJFOC-20160704542 JANSSEN 0.00 C M Y 0.00000 20160829 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
126940441 12694044 1 SS CONCERTA METHYLPHENIDATE HYDROCHLORIDE 1 Oral U U UNKNOWN 0 36 MG SUSTAINED RELEASE TABLETS QD
126940441 12694044 2 PS CONCERTA METHYLPHENIDATE HYDROCHLORIDE 1 Oral U U UNKNOWN 21121 SUSTAINED RELEASE TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126940441 12694044 1 Attention deficit/hyperactivity disorder
126940441 12694044 2 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126940441 12694044 Decreased appetite
126940441 12694044 Disturbance in attention
126940441 12694044 Drug ineffective
126940441 12694044 Fatigue
126940441 12694044 Hunger
126940441 12694044 Insomnia

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
126940441 12694044 1 2015 0