The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6767570 7418343 I 6767570-X 20100601 20100614 EXP PHHY2010CA36856 NOVARTIS PHARMACEUTICAL CORPORATION YR M Y 20100614 CANADA

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6767570 1013857272 PS CLOZARIL 1 450 MG HS (CRUSHED) 019758
6767570 1013857273 C OMEGA-3 FATTY ACIDS 2 3000 MG
6767570 1013857274 C OLANZAPINE 1 5 MG HS
6767570 1013857275 C DOCUSATE SODIUM 2 100 MG, BID
6767570 1013857276 C PANTOPRAZOLE SODIUM 1 40 MG
6767570 1013857277 C QUETIAPINE FUMARATE 1 25 MG Q4H PRN
6767570 1013857278 C LORAZEPAM 1 ORAL 1-2 MG TID PRN
6767570 1013857279 C RABEPRAZOLE SODIUM 1 20 MG
6767570 1013857280 C DOCUSATE CALCIUM 2 450 MG DAILY

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
6767570 OT

Reactions reported

Event ID PT
6767570 AGRANULOCYTOSIS
6767570 CHOLELITHIASIS
6767570 HEPATIC CYST
6767570 NEUTROPHIL COUNT DECREASED
6767570 WHITE BLOOD CELL COUNT DECREASED

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6767570 1013857272 20080408 20100525 778 DAY
6767570 1013857273 20100526
6767570 1013857274 20100514 20100526 13 DAY
6767570 1013857275 20100514
6767570 1013857276 20100526
6767570 1013857277 20100527
6767570 1013857278 20100514 20100526 13 DAY
6767570 1013857279 20100514