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
74803553 7480355 3 F 20130918 20130924 20100716 20130930 EXP PHHY2008AU36970 NOVARTIS 38.17 YR M Y 94.00000 KG 20130930 MD 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
74803553 7480355 1 PS CLOZARIL 1 ORAL 850 MG U 19758 850 MG TABLET
74803553 7480355 2 SS CLOZARIL 1 UNK U 19758 TABLET
74803553 7480355 3 SS CLOZARIL 1 UNK U 19758 TABLET
74803553 7480355 4 SS CLOZARIL 1 550 MG U 19758 550 MG TABLET
74803553 7480355 5 C DIAZEPAM 1 ORAL 5 MG, PRN U 0 5 MG
74803553 7480355 6 C ESCITALOPRAM 1 ORAL 20 MG, DAILY U 0 20 MG
74803553 7480355 7 C AMISULPRIDE 1 200 MG, BID U 0 200 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
74803553 7480355 1 Schizophrenia

Outcome of event

Event ID CASEID OUTC COD
74803553 7480355 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
74803553 7480355 Cardiac disorder
74803553 7480355 Echocardiogram abnormal
74803553 7480355 Electrocardiogram QT prolonged
74803553 7480355 Left ventricular dysfunction
74803553 7480355 Libido decreased
74803553 7480355 Myocarditis
74803553 7480355 Sexual dysfunction

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
74803553 7480355 1 20040715 0
74803553 7480355 2 20071022 0
74803553 7480355 4 20130918 0
74803553 7480355 5 20120605 0
74803553 7480355 6 20110511 0
74803553 7480355 7 20130919 0