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
111186745 11118674 5 F 2006 20160610 20150518 20160830 PER US-JNJFOC-20150508742 JANSSEN 0.00 C M Y 0.00000 20160830 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
111186745 11118674 1 SS RISPERDAL RISPERIDONE 1 Oral U U 0 .5 MG UNSPECIFIED
111186745 11118674 2 SS RISPERDAL RISPERIDONE 1 Oral U U 0 1 MG UNSPECIFIED
111186745 11118674 3 SS RISPERDAL RISPERIDONE 1 Oral U U 0 3 MG UNSPECIFIED
111186745 11118674 4 SS RISPERDAL RISPERIDONE 1 Oral U U 0 1 MG UNSPECIFIED
111186745 11118674 5 SS RISPERDAL RISPERIDONE 1 Oral U U 0 3 MG UNSPECIFIED
111186745 11118674 6 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 .5 MG UNSPECIFIED
111186745 11118674 7 SS RISPERIDONE. RISPERIDONE 1 Oral U U 0 .75 MG UNSPECIFIED
111186745 11118674 8 SS RISPERIDONE. RISPERIDONE 1 Oral U U 0 1.5 MG UNSPECIFIED
111186745 11118674 9 SS RISPERIDONE. RISPERIDONE 1 Oral U U 0 1.5 MG UNSPECIFIED
111186745 11118674 10 SS RISPERIDONE. RISPERIDONE 1 Oral U U 20272 .75 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111186745 11118674 1 Attention deficit/hyperactivity disorder
111186745 11118674 2 Attention deficit/hyperactivity disorder
111186745 11118674 3 Attention deficit/hyperactivity disorder
111186745 11118674 4 Bipolar disorder
111186745 11118674 5 Bipolar disorder
111186745 11118674 6 Bipolar disorder
111186745 11118674 7 Attention deficit/hyperactivity disorder
111186745 11118674 8 Attention deficit/hyperactivity disorder
111186745 11118674 9 Bipolar disorder
111186745 11118674 10 Bipolar disorder

Outcome of event

Event ID CASEID OUTC COD
111186745 11118674 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
111186745 11118674 Abnormal weight gain
111186745 11118674 Gynaecomastia
111186745 11118674 Hyperprolactinaemia

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
111186745 11118674 1 20091109 0
111186745 11118674 2 20060612 20060705 0
111186745 11118674 3 20101214 20110626 0
111186745 11118674 4 20060612 20060705 0
111186745 11118674 5 20101214 20110626 0
111186745 11118674 6 20091109 0
111186745 11118674 7 20091109 20091209 0
111186745 11118674 8 20101214 20110721 0
111186745 11118674 9 20101214 20110721 0
111186745 11118674 10 20091109 20091209 0