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
109323444 10932344 4 F 2009 20160628 20150320 20160830 PER US-JNJFOC-20140700391 JANSSEN 49.92 YR A 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
109323444 10932344 1 PS RISPERDAL RISPERIDONE 1 Oral N U 20272 5 MG UNSPECIFIED
109323444 10932344 2 SS RISPERIDONE. RISPERIDONE 1 Oral U U 20272 TABLETS
109323444 10932344 3 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109323444 10932344 1 Schizophrenia
109323444 10932344 2 Product used for unknown indication
109323444 10932344 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
109323444 10932344 Breast discharge
109323444 10932344 Breast swelling
109323444 10932344 Extrapyramidal disorder
109323444 10932344 Feeling abnormal
109323444 10932344 Gastric disorder
109323444 10932344 Gynaecomastia
109323444 10932344 Pain
109323444 10932344 Sedation
109323444 10932344 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
109323444 10932344 1 2008 2013 0