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
118174082 11817408 2 F 200711 20160622 20151210 20160830 PER US-JNJFOC-20150703017 JANSSEN 27.73 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
118174082 11817408 1 SS RISPERDAL RISPERIDONE 1 Oral U U 0 UNSPECIFIED
118174082 11817408 2 SS RISPERDAL RISPERIDONE 1 Oral U U 0 UNSPECIFIED
118174082 11817408 3 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118174082 11817408 1 Tourette's disorder
118174082 11817408 2 Tourette's disorder
118174082 11817408 3 Tourette's disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118174082 11817408 Abnormal weight gain
118174082 11817408 Anxiety
118174082 11817408 Depression
118174082 11817408 Extrapyramidal disorder
118174082 11817408 Galactorrhoea
118174082 11817408 Gynaecomastia
118174082 11817408 Hyperprolactinaemia
118174082 11817408 Off label use
118174082 11817408 Product use issue

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
118174082 11817408 1 200803 200808 0
118174082 11817408 2 200711 200712 0
118174082 11817408 3 201007 201008 0