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
117356282 11735628 2 F 2006 20160912 20151113 20160929 PER US-JNJFOC-20151004597 JANSSEN 0.00 C M Y 0.00000 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
117356282 11735628 1 SS RISPERDAL RISPERIDONE 1 Unknown U 0 .5 MG TABLETS
117356282 11735628 2 PS RISPERDAL RISPERIDONE 1 Unknown U 20272 .5 MG TABLETS
117356282 11735628 3 SS INVEGA PALIPERIDONE 1 Oral 3-6 MG U 0 OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET
117356282 11735628 4 SS INVEGA PALIPERIDONE 1 Oral 3-6 MG U 21999 OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117356282 11735628 1 Bipolar disorder
117356282 11735628 2 Attention deficit/hyperactivity disorder
117356282 11735628 3 Bipolar disorder
117356282 11735628 4 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
117356282 11735628 Blood prolactin increased
117356282 11735628 Emotional disorder
117356282 11735628 Gynaecomastia
117356282 11735628 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
117356282 11735628 1 200505 200612 0
117356282 11735628 2 200505 200612 0
117356282 11735628 3 2009 201312 0
117356282 11735628 4 2009 201312 0