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
126306961 12630696 1 I 20150518 20160728 20160808 20160808 EXP IT-ELI_LILLY_AND_COMPANY-IT201607013403 ELI LILLY AND CO 74.71 YR M Y 0.00000 20160805 CN IT IT

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
126306961 12630696 1 PS HUMALOG INSULIN LISPRO 1 Subcutaneous 19 IU, QD U U 20563 19 IU INJECTION QD
126306961 12630696 2 SS LANTUS INSULIN GLARGINE 1 Subcutaneous 20 IU, QD U U 0 20 IU INJECTION QD
126306961 12630696 3 C PANTORC PANTOPRAZOLE SODIUM 1 U 0
126306961 12630696 4 C LASIX FUROSEMIDE 1 U 0 TABLET
126306961 12630696 5 C STILNOX ZOLPIDEM TARTRATE 1 U 0
126306961 12630696 6 C CARDIOASPIRINA ASPIRIN 1 U 0
126306961 12630696 7 C FLUXUM PARNAPARIN SODIUM 1 U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126306961 12630696 1 Product used for unknown indication
126306961 12630696 2 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126306961 12630696 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126306961 12630696 Compensatory sweating
126306961 12630696 Hypoglycaemia

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

no results found

Therapies reported

no results found