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
127439212 12743921 2 F 201609 20160909 20160914 20160921 EXP US-ELI_LILLY_AND_COMPANY-US201609002291 ELI LILLY AND CO 0.00 F Y 0.00000 20160921 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
127439212 12743921 1 PS HUMULIN N INSULIN HUMAN 1 Unknown UNK, UNKNOWN Y U 18780 INJECTION
127439212 12743921 2 SS HUMULIN N INSULIN HUMAN 1 Unknown UNK, UNKNOWN Y U C462153C 18780 INJECTION
127439212 12743921 3 SS HUMULIN N INSULIN HUMAN 1 Unknown UNK, UNKNOWN Y U C494907C 18780 INJECTION
127439212 12743921 4 SS HUMULIN N INSULIN HUMAN 1 Unknown UNK, UNKNOWN Y U 18780 INJECTION
127439212 12743921 5 SS HUMULIN R INSULIN HUMAN 1 Unknown UNK, UNKNOWN 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127439212 12743921 1 Type 1 diabetes mellitus
127439212 12743921 5 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127439212 12743921 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127439212 12743921 Anaphylactic shock
127439212 12743921 Blood glucose decreased
127439212 12743921 Blood glucose increased
127439212 12743921 Drug hypersensitivity
127439212 12743921 Eye disorder
127439212 12743921 Urticaria

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
127439212 12743921 1 1996 0
127439212 12743921 4 20160904 0
127439212 12743921 5 1996 0