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
88599272 8859927 2 F 2001 20160822 20121025 20160830 EXP US-ELI_LILLY_AND_COMPANY-US201210003578 ELI LILLY AND CO 0.00 M Y 0.00000 20160829 CN US US

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
88599272 8859927 1 PS ZYPREXA OLANZAPINE 1 Unknown 10 MG, QD Y U 20592 10 MG TABLET QD
88599272 8859927 2 SS ZYPREXA OLANZAPINE 1 Unknown 5 MG, QD Y U 20592 5 MG TABLET QD
88599272 8859927 3 SS ZYPREXA OLANZAPINE 1 Unknown 1 DF, PRN Y U 20592 1 DF TABLET
88599272 8859927 4 C PROLIXIN FLUPHENAZINE HYDROCHLORIDE 1 Unknown UNK, UNKNOWN U 0
88599272 8859927 5 C RISPERIDONE. RISPERIDONE 1 Unknown UNK, UNKNOWN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
88599272 8859927 1 Confusional state

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
88599272 8859927 Blister
88599272 8859927 Body temperature increased
88599272 8859927 Cough
88599272 8859927 Depression
88599272 8859927 Epistaxis
88599272 8859927 Fatigue
88599272 8859927 Malaise
88599272 8859927 Off label use
88599272 8859927 Platelet count decreased
88599272 8859927 Pollakiuria
88599272 8859927 Somnolence

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
88599272 8859927 1 1997 0
88599272 8859927 2 20040301 0