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
127877521 12787752 1 I 20160920 20160928 20160928 EXP TR-ASTRAZENECA-2016SF00945 ASTRAZENECA 0.00 T F Y 0.00000 20160928 MD TR TR

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
127877521 12787752 1 PS QUETIAPINE. QUETIAPINE 1 Oral U U 20639 TABLET
127877521 12787752 2 SS RISPERIDONE. RISPERIDONE 1 Unknown U 0
127877521 12787752 3 C ARIPIPRAZOLE. ARIPIPRAZOLE 1 Unknown 0
127877521 12787752 4 C AMISULPRIDE AMISULPRIDE 1 Unknown 0
127877521 12787752 5 C FLUOXETINE FLUOXETINE HYDROCHLORIDE 1 Unknown 0
127877521 12787752 6 C OLANZAPINE. OLANZAPINE 1 Unknown 0
127877521 12787752 7 C LORAZEPAM. LORAZEPAM 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127877521 12787752 1 Mutism
127877521 12787752 3 Mutism
127877521 12787752 4 Mutism
127877521 12787752 5 Mutism
127877521 12787752 6 Mutism
127877521 12787752 7 Mutism

Outcome of event

Event ID CASEID OUTC COD
127877521 12787752 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127877521 12787752 Neutropenia
127877521 12787752 Off label use
127877521 12787752 Product use issue

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

no results found

Therapies reported

no results found