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
127871581 12787158 1 I 2010 20160915 20160927 20160927 EXP US-ELI_LILLY_AND_COMPANY-US201609006323 ELI LILLY AND CO 0.00 F Y 0.00000 20160927 CN US US

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
127871581 12787158 1 PS HUMULIN N INSULIN HUMAN 1 Unknown 38 U, EACH MORNING C518703E 18780 38 IU INJECTION QD
127871581 12787158 2 SS HUMULIN N INSULIN HUMAN 1 Unknown UNK, PRN C518703E 18780 INJECTION
127871581 12787158 3 SS HUMULIN N INSULIN HUMAN 1 Unknown UNK, PRN C518703E 18780 INJECTION
127871581 12787158 4 SS HUMULIN R INSULIN HUMAN 1 Unknown 3 U, AT DINNER C581151A 0 3 IU INJECTION
127871581 12787158 5 SS HUMULIN R INSULIN HUMAN 1 Unknown 28 U, AT BEDTIME C581151A 0 28 IU INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127871581 12787158 1 Type 2 diabetes mellitus
127871581 12787158 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127871581 12787158 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127871581 12787158 Arthralgia
127871581 12787158 Back pain
127871581 12787158 Bladder disorder
127871581 12787158 Blood glucose abnormal
127871581 12787158 Foot fracture
127871581 12787158 Limb discomfort
127871581 12787158 Limb mass
127871581 12787158 Pain
127871581 12787158 Renal disorder
127871581 12787158 Seizure
127871581 12787158 Soft tissue disorder

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

no results found

Therapies reported

no results found