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
104726702 10472670 2 F 20160912 20140924 20160923 EXP MX-ELI_LILLY_AND_COMPANY-MX201409006769 ELI LILLY AND CO 0.00 F Y 78.00000 KG 20160923 CN MX MX

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
104726702 10472670 1 PS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 48 DF, EACH MORNING U 20563 48 DF QD
104726702 10472670 2 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 24 DF, EACH EVENING U 20563 24 DF QD
104726702 10472670 3 SS HUMALOG INSULIN LISPRO 1 Unknown 12 U, QD U 0 12 IU QD
104726702 10472670 4 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown UNK, UNKNOWN U U 0 INJECTION
104726702 10472670 5 SS HUMALOG INSULIN LISPRO 1 U U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104726702 10472670 1 Product used for unknown indication
104726702 10472670 3 Product used for unknown indication
104726702 10472670 4 Product used for unknown indication
104726702 10472670 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
104726702 10472670 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
104726702 10472670 Arthropathy
104726702 10472670 Feeling abnormal
104726702 10472670 Hyperglycaemia
104726702 10472670 Injection site pain
104726702 10472670 Oral pain
104726702 10472670 Pericoronitis

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
104726702 10472670 1 20140831 0
104726702 10472670 2 20140831 0
104726702 10472670 3 20140831 0