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
126577381 12657738 1 I 20160808 20160816 20160816 EXP CN-ELI_LILLY_AND_COMPANY-CN201608006620 ELI LILLY AND CO 0.00 F Y 0.00000 20160816 CN CN CN

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
126577381 12657738 1 PS ZYPREXA OLANZAPINE 1 Oral 1.67 MG, QD Y U C355407 20592 1.67 MG TABLET QD
126577381 12657738 2 SS ZYPREXA OLANZAPINE 1 Y U 20592 TABLET
126577381 12657738 3 C GABAPENTIN. GABAPENTIN 1 Oral 300 MG, QD 20151102 0 300 MG QD
126577381 12657738 4 C PRAMIPEXOLE. PRAMIPEXOLE 1 Unknown 0.25 MG, QD 0 .25 MG QD
126577381 12657738 5 C CLONAZEPAM. CLONAZEPAM 1 Unknown 1 MG, QD 0 1 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126577381 12657738 1 Sleep disorder
126577381 12657738 2 Restless legs syndrome
126577381 12657738 3 Restless legs syndrome
126577381 12657738 4 Restless legs syndrome
126577381 12657738 5 Restless legs syndrome

Outcome of event

Event ID CASEID OUTC COD
126577381 12657738 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126577381 12657738 Face oedema
126577381 12657738 Oedema peripheral
126577381 12657738 Off label use
126577381 12657738 Underdose

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
126577381 12657738 1 20160117 20160126 0