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
100643283 10064328 3 F 20140121 20160622 20140408 20160630 EXP JP-ELI_LILLY_AND_COMPANY-JP201404001003 ELI LILLY AND CO 70.36 YR F Y 0.00000 20160630 OT JP JP

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
100643283 10064328 1 PS ZYPREXA OLANZAPINE 1 Oral UNK 20592 DISPERSIBLE TABLET
100643283 10064328 2 SS ZYPREXA OLANZAPINE 1 20592 DISPERSIBLE TABLET
100643283 10064328 3 C FENTANYL /00174602/ FENTANYL 1 Transdermal UNK 0
100643283 10064328 4 C MAGLAX MAGNESIUM OXIDE 1 Oral 330 MG, TID 0 330 MG TID
100643283 10064328 5 C LAXOBERON SODIUM PICOSULFATE 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100643283 10064328 1 Nausea
100643283 10064328 2 Decreased appetite
100643283 10064328 3 Cancer pain
100643283 10064328 4 Constipation
100643283 10064328 5 Constipation

Outcome of event

Event ID CASEID OUTC COD
100643283 10064328 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100643283 10064328 Delirium
100643283 10064328 Off label use

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
100643283 10064328 1 20140121 20140202 0
100643283 10064328 3 201312 0
100643283 10064328 4 20140121 0
100643283 10064328 5 20140121 0