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
1031139424 10311394 24 F 20140714 20150624 20140717 20150630 EXP PHFR2014GB004833 NOVARTIS 61.25 YR M Y 0.00000 20150630 N OT GB GB

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
1031139424 10311394 1 PS CLOZARIL CLOZAPINE 1 Oral 350 MG, QD D 19758 350 MG TABLET QD
1031139424 10311394 2 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 20 MG, QD D 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1031139424 10311394 1 Schizophrenia
1031139424 10311394 2 Peptic ulcer

Outcome of event

Event ID CASEID OUTC COD
1031139424 10311394 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1031139424 10311394 Chronic lymphocytic leukaemia
1031139424 10311394 Haemoglobin decreased
1031139424 10311394 Neutrophil count decreased
1031139424 10311394 Platelet count decreased
1031139424 10311394 Speech disorder
1031139424 10311394 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 CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
1031139424 10311394 1 20140708 0
1031139424 10311394 2 20140709 0