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
126647621 12664762 1 I 20160810 20160818 20160818 EXP PHHY2016AU111301 SANDOZ 0.00 M Y 0.00000 20160818 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
126647621 12664762 1 SS CLOZARIL CLOZAPINE 1 Unknown U 0
126647621 12664762 2 PS OLANZAPINE. OLANZAPINE 1 Unknown U 201588
126647621 12664762 3 SS HALOPERIDOL. HALOPERIDOL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126647621 12664762 1 Product used for unknown indication
126647621 12664762 2 Product used for unknown indication
126647621 12664762 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126647621 12664762 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126647621 12664762 Aspartate aminotransferase increased
126647621 12664762 Bilirubin conjugated increased
126647621 12664762 Blood bicarbonate decreased
126647621 12664762 Blood bilirubin increased
126647621 12664762 Blood creatine decreased
126647621 12664762 Blood glucose increased
126647621 12664762 Blood lactate dehydrogenase increased
126647621 12664762 Blood sodium decreased
126647621 12664762 Blood uric acid increased
126647621 12664762 Cardiac disorder
126647621 12664762 Cardiomyopathy
126647621 12664762 Echocardiogram abnormal
126647621 12664762 Globulins decreased
126647621 12664762 Psychiatric decompensation
126647621 12664762 Tachycardia

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

no results found

Therapies reported

no results found