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
126223761 12622376 1 I 20160802 20160804 20160804 EXP AU-ASTRAZENECA-2016SE83648 ASTRAZENECA 31.00 YR M Y 0.00000 20160804 OT AU AU

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
126223761 12622376 1 PS QUETIAPINE. QUETIAPINE 1 Oral U 20639 TABLET

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126223761 12622376 DE
126223761 12622376 OT
126223761 12622376 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126223761 12622376 Cardiac arrest
126223761 12622376 Depressed level of consciousness
126223761 12622376 Overdose
126223761 12622376 Respiratory depression
126223761 12622376 Seizure

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

no results found

Therapies reported

no results found