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
64792644 6479264 4 F 2000 20160913 20071203 20160920 EXP FR-ELI_LILLY_AND_COMPANY-FR200711005833 ELI LILLY AND CO 0.00 M Y 125.00000 KG 20160920 MD FR FR

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
64792644 6479264 1 PS ZYPREXA OLANZAPINE 1 Oral 1 DF, UNKNOWN U U 20592 1 DF TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
64792644 6479264 1 Autism

Outcome of event

Event ID CASEID OUTC COD
64792644 6479264 HO
64792644 6479264 DS
64792644 6479264 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
64792644 6479264 Aggression
64792644 6479264 Agitation
64792644 6479264 Anxiety
64792644 6479264 Benign prostatic hyperplasia
64792644 6479264 Blindness unilateral
64792644 6479264 Diabetes mellitus
64792644 6479264 Dry mouth
64792644 6479264 Dysuria
64792644 6479264 Headache
64792644 6479264 Heart rate increased
64792644 6479264 Hyperphagia
64792644 6479264 Initial insomnia
64792644 6479264 Mental disorder
64792644 6479264 Micturition disorder
64792644 6479264 Obesity
64792644 6479264 Off label use
64792644 6479264 Panic attack
64792644 6479264 Pollakiuria
64792644 6479264 Skin disorder
64792644 6479264 Somnolence
64792644 6479264 Thirst
64792644 6479264 Urinary incontinence
64792644 6479264 Weight increased

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
64792644 6479264 1 2000 0