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
126751001 12675100 1 I 2016 20160810 20160822 20160822 EXP US-ELI_LILLY_AND_COMPANY-US201608006868 ELI LILLY AND CO 0.00 F Y 0.00000 20160822 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
126751001 12675100 1 PS HUMALOG INSULIN LISPRO 1 Subcutaneous UNK, UNKNOWN UNKNOWN 20563 INJECTION
126751001 12675100 2 SS HUMALOG INSULIN LISPRO 1 Subcutaneous UNK, UNKNOWN C536215A 20563 INJECTION
126751001 12675100 3 SS HUMALOG INSULIN LISPRO 1 Subcutaneous UNK, UNKNOWN (NOT USED YET) C531767A 20563 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126751001 12675100 1 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126751001 12675100 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126751001 12675100 Acidosis
126751001 12675100 Blood glucose increased
126751001 12675100 Flatulence
126751001 12675100 Headache
126751001 12675100 Hypoglycaemia
126751001 12675100 Incorrect product storage
126751001 12675100 Malaise
126751001 12675100 Nausea
126751001 12675100 Pollakiuria

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
126751001 12675100 1 201606 0
126751001 12675100 2 2016 0