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
127288181 12728818 1 I 201602 20160829 20160909 20160909 EXP BR-ELI_LILLY_AND_COMPANY-BR201608013636 ELI LILLY AND CO 51.99 YR M Y 100.00000 KG 20160909 CN BR BR

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
127288181 12728818 1 PS HUMULIN N INSULIN HUMAN 1 Unknown 35 IU, BID 18780 35 IU INJECTION BID
127288181 12728818 2 SS HUMULIN N INSULIN HUMAN 1 Unknown 20 IU, EACH EVENING 18780 20 IU INJECTION QD
127288181 12728818 3 SS HUMULIN N INSULIN HUMAN 1 Unknown 35 IU, BID C572615D 18780 35 IU INJECTION BID
127288181 12728818 4 SS HUMULIN N INSULIN HUMAN 1 Unknown 20 IU, EACH EVENING C572615D 18780 20 IU INJECTION QD
127288181 12728818 5 C APIDRA INSULIN GLULISINE 1 Unknown UNK, UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127288181 12728818 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127288181 12728818 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127288181 12728818 Blood glucose increased
127288181 12728818 Localised infection
127288181 12728818 Visual acuity reduced

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

no results found

Therapies reported

no results found