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
127845711 12784571 1 I 2001 20160923 20160927 20160927 EXP BR-JNJFOC-20160925704 JANSSEN 0.00 A M Y 0.00000 20160927 CN BR BR

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
127845711 12784571 1 PS RISPERIDONE. RISPERIDONE 1 Unknown U U UNKNOWN 20272 UNSPECIFIED
127845711 12784571 2 C HALDOL HALOPERIDOL 1 Unknown D 0 TABLETS
127845711 12784571 3 C LITHIUM CARBONATE. LITHIUM CARBONATE 1 Unknown D 0 UNSPECIFIED
127845711 12784571 4 C AKINETON BIPERIDEN HYDROCHLORIDE 1 Unknown D 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127845711 12784571 1 Product used for unknown indication
127845711 12784571 2 Major depression

Outcome of event

Event ID CASEID OUTC COD
127845711 12784571 HO
127845711 12784571 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127845711 12784571 Blood pressure increased
127845711 12784571 Hospitalisation
127845711 12784571 Hunger
127845711 12784571 Psychotic disorder

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
127845711 12784571 1 2001 0
127845711 12784571 2 1999 0