The Safety Rates Drug Report

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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
125360021 12536002 1 I 20160627 20160707 20160707 PER US-ELI_LILLY_AND_COMPANY-US201606009915 ELI LILLY AND CO 0.00 M Y 0.00000 20160707 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
125360021 12536002 1 PS ZYPREXA OLANZAPINE 1 Unknown 10 MG, QID 20592 10 MG TABLET QID
125360021 12536002 2 SS ZYPREXA OLANZAPINE 1 Unknown 15 MG, QID 20592 15 MG TABLET QID
125360021 12536002 3 SS ZYPREXA OLANZAPINE 1 20592 TABLET
125360021 12536002 4 C FLUVOXAMINE MALEATE. FLUVOXAMINE MALEATE 1 Unknown UNK UNK, UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125360021 12536002 1 Panic attack
125360021 12536002 2 Antisocial behaviour
125360021 12536002 3 Paranoia
125360021 12536002 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125360021 12536002 Libido decreased
125360021 12536002 Prescribed overdose

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

no results found

Therapies reported

no results found