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
125517201 12551720 1 I 20150811 20160713 20160713 PER US-TEVA-586052USA TEVA 0.00 M Y 33.00000 KG 20160713 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
125517201 12551720 1 PS RISPERIDONE. RISPERIDONE 1 Unknown AT 4 O'CLOCK U 77769 5 MG TABLET
125517201 12551720 2 I QUILLIVANT XR METHYLPHENIDATE HYDROCHLORIDE 1 Oral ONCE IN AM N 0
125517201 12551720 3 SS CLONIDINE. CLONIDINE 1 Unknown ONCE AT BED TIME U 0 1 MG TABLET
125517201 12551720 4 SS DEPAKOTE DIVALPROEX SODIUM 1 Unknown ONE IN THE MORNING AT 8 AND AT NOON U 0 250 MG TABLET
125517201 12551720 5 SS DEPAKOTE DIVALPROEX SODIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125517201 12551720 1 Depression
125517201 12551720 2 Attention deficit/hyperactivity disorder
125517201 12551720 3 Depression
125517201 12551720 4 Depression
125517201 12551720 5 Affective disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125517201 12551720 Abdominal pain upper
125517201 12551720 Drug interaction
125517201 12551720 Irritability

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
125517201 12551720 2 20150508 20150525 0