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
125734701 12573470 1 I 2006 20160708 20160720 20160720 EXP BR-ELI_LILLY_AND_COMPANY-BR201607003154 ELI LILLY AND CO 0.00 M Y 95.00000 KG 20160720 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
125734701 12573470 1 PS HUMULIN N INSULIN HUMAN 1 Unknown 22 IU, EACH MORNING U U 18780 22 IU INJECTION QD
125734701 12573470 2 SS HUMULIN N INSULIN HUMAN 1 Unknown 10 IU, IN THE AFTERNOON U U 18780 10 IU INJECTION
125734701 12573470 3 SS HUMULIN N INSULIN HUMAN 1 Unknown 26 IU, EACH EVENING U U 18780 26 IU INJECTION QD
125734701 12573470 4 SS HUMULIN N INSULIN HUMAN 1 Unknown 22 IU, EACH MORNING U U C326605D 18780 22 IU INJECTION QD
125734701 12573470 5 SS HUMULIN N INSULIN HUMAN 1 Unknown 10 IU, IN THE AFTERNOON U U C326605D 18780 10 IU INJECTION
125734701 12573470 6 SS HUMULIN N INSULIN HUMAN 1 Unknown 26 IU, EACH EVENING U U C326605D 18780 26 IU INJECTION QD
125734701 12573470 7 SS HUMULIN R INSULIN HUMAN 1 Unknown 14 IU, EACH MORNING U U 0 14 IU INJECTION QD
125734701 12573470 8 SS HUMULIN R INSULIN HUMAN 1 Unknown 10 IU, IN THE AFTERNOON U U 0 10 IU INJECTION
125734701 12573470 9 SS HUMULIN R INSULIN HUMAN 1 Unknown 16 IU, EACH EVENING U U 0 16 IU INJECTION QD
125734701 12573470 10 SS HUMULIN R INSULIN HUMAN 1 Unknown 14 IU, EACH MORNING U U C514127H 0 14 IU INJECTION QD
125734701 12573470 11 SS HUMULIN R INSULIN HUMAN 1 Unknown 10 IU, IN THE AFTERNOON U U C514127H 0 10 IU INJECTION
125734701 12573470 12 SS HUMULIN R INSULIN HUMAN 1 Unknown 16 IU, EACH EVENING U U C514127H 0 16 IU INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125734701 12573470 1 Type 2 diabetes mellitus
125734701 12573470 7 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125734701 12573470 OT
125734701 12573470 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125734701 12573470 Blindness
125734701 12573470 Diabetic neuropathy
125734701 12573470 Incorrect product storage

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
125734701 12573470 1 2004 0
125734701 12573470 2 2004 0
125734701 12573470 3 2004 0
125734701 12573470 7 2004 0
125734701 12573470 8 2004 0
125734701 12573470 9 2004 0