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
112827913 11282791 3 F 20160825 20150720 20160905 EXP US-JNJFOC-20150713517 JANSSEN 0.00 M Y 0.00000 20160905 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
112827913 11282791 1 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 UNSPECIFIED
112827913 11282791 2 SS RISPERIDONE. RISPERIDONE 1 Oral VARYING DOSES OF 4MG AND 1MG U 0 TABLET
112827913 11282791 3 SS INVEGA PALIPERIDONE 1 Oral U U 21999 OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112827913 11282791 1 Product used for unknown indication
112827913 11282791 2 Product used for unknown indication
112827913 11282791 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
112827913 11282791 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112827913 11282791 Abnormal weight gain
112827913 11282791 Diabetes mellitus
112827913 11282791 Gynaecomastia
112827913 11282791 Homicidal ideation
112827913 11282791 Hyperprolactinaemia

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

no results found

Therapies reported

no results found