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
126456101 12645610 1 I 2007 20160803 20160811 20160811 EXP BR-ELI_LILLY_AND_COMPANY-BR201608002618 ELI LILLY AND CO 0.00 F Y 0.00000 20160810 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
126456101 12645610 1 PS Insulin Human INSULIN HUMAN 1 Unknown 40 IU, EACH MORNING U U 18780 40 IU QD
126456101 12645610 2 SS Insulin Human INSULIN HUMAN 1 Unknown UNK, EACH EVENING U U 18780 QD
126456101 12645610 3 SS HUMULIN N INSULIN HUMAN 1 Unknown 40 IU, EACH MORNING U U 0 40 IU QD
126456101 12645610 4 SS HUMULIN N INSULIN HUMAN 1 Unknown UNK, EACH EVENING U U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126456101 12645610 1 Product used for unknown indication
126456101 12645610 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126456101 12645610 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126456101 12645610 Administration site necrosis
126456101 12645610 Blood glucose increased
126456101 12645610 Fibromyalgia
126456101 12645610 Headache
126456101 12645610 Hepatic steatosis
126456101 12645610 Injection site bruising
126456101 12645610 Nephrolithiasis

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

no results found

Therapies reported

no results found