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
126716612 12671661 2 F 2014 20160905 20160822 20160929 PER US-JNJFOC-20160719981 JANSSEN 0.00 A F Y 90.72000 KG 20160929 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
126716612 12671661 1 SS RISPERIDONE. RISPERIDONE 1 Oral Y N UNKNOWN 0 TABLETS
126716612 12671661 2 PS RISPERIDONE. RISPERIDONE 1 Oral Y N UNKNOWN 20272 TABLETS
126716612 12671661 3 SS INVEGA SUSTENNA PALIPERIDONE PALMITATE 1 Unknown N 22264 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126716612 12671661 1 Schizophrenia
126716612 12671661 2 Schizophrenia
126716612 12671661 3 Schizophrenia

Outcome of event

Event ID CASEID OUTC COD
126716612 12671661 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126716612 12671661 Abdominal pain upper
126716612 12671661 Adverse drug reaction
126716612 12671661 Hallucination
126716612 12671661 Headache
126716612 12671661 Ill-defined disorder
126716612 12671661 Thinking abnormal
126716612 12671661 Treatment noncompliance

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
126716612 12671661 1 201403 201408 0
126716612 12671661 2 201411 201411 0
126716612 12671661 3 201411 0