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
69425012 6942501 2 F 20160915 20090317 20160920 EXP US-JNJFOC-20090303170 JANSSEN 0.00 M Y 0.00000 20160920 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
69425012 6942501 1 PS RISPERDAL RISPERIDONE 1 Unknown U U 20272 UNSPECIFIED
69425012 6942501 2 SS HALDOL HALOPERIDOL 1 Unknown U U 15923 UNSPECIFIED
69425012 6942501 3 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 TABLET
69425012 6942501 4 SS ZYPREXA OLANZAPINE 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
69425012 6942501 1 Product used for unknown indication
69425012 6942501 2 Product used for unknown indication
69425012 6942501 3 Product used for unknown indication
69425012 6942501 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
69425012 6942501 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
69425012 6942501 Cardiac disorder
69425012 6942501 Disturbance in attention
69425012 6942501 Hallucination, auditory
69425012 6942501 Nausea
69425012 6942501 Sleep disorder
69425012 6942501 Vomiting
69425012 6942501 Weight increased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found