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
126095981 12609598 1 I 20160719 20160801 20160801 EXP DK-PAR PHARMACEUTICAL COMPANIES-2016SCPR015677 PAR 0.00 Y 0.00000 20160801 OT DK DK

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
126095981 12609598 1 PS OLANZAPINE. OLANZAPINE 1 Unknown 20 MG / DAY 78109 20 MG QD
126095981 12609598 2 SS OLANZAPINE. OLANZAPINE 1 Unknown 5 MG, PRN 78109 5 MG
126095981 12609598 3 SS ARIPIPRAZOLE. ARIPIPRAZOLE 1 Unknown 30 MG / DAY 0 30 MG QD
126095981 12609598 4 SS MIRTAZAPINE. MIRTAZAPINE 1 Unknown 30 MG / DAY 0 30 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126095981 12609598 1 Product used for unknown indication
126095981 12609598 3 Product used for unknown indication
126095981 12609598 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126095981 12609598 OT
126095981 12609598 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126095981 12609598 Eosinophilic myocarditis
126095981 12609598 Overdose

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

no results found

Therapies reported

no results found