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
109514505 10951450 5 F 20160802 20150324 20160830 PER US-JNJFOC-20130510743 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
109514505 10951450 1 PS RISPERDAL RISPERIDONE 1 Oral U 20272 TABLETS
109514505 10951450 2 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 UNSPECIFIED
109514505 10951450 3 SS RISPERIDONE. RISPERIDONE 1 Oral U 20272 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109514505 10951450 1 Affect lability
109514505 10951450 2 Anxiety
109514505 10951450 3 Affective disorder

Outcome of event

Event ID CASEID OUTC COD
109514505 10951450 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
109514505 10951450 Blood prolactin increased
109514505 10951450 Breast pain
109514505 10951450 Depression
109514505 10951450 Emotional distress
109514505 10951450 Gynaecomastia
109514505 10951450 Weight increased

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
109514505 10951450 2 2004 2010 0
109514505 10951450 3 2004 2010 0