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
126576641 12657664 1 I 20160808 20160816 20160816 EXP BR-ELI_LILLY_AND_COMPANY-BR201608005290 ELI LILLY AND CO 0.00 M Y 72.00000 KG 20160816 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
126576641 12657664 1 PS HUMULIN N INSULIN HUMAN 1 Subcutaneous 34 IU, EACH MORNING 18780 34 IU INJECTION QD
126576641 12657664 2 SS HUMULIN N INSULIN HUMAN 1 Subcutaneous 12 IU, EACH EVENING 18780 12 IU INJECTION QD
126576641 12657664 3 C DIOVAN VALSARTAN 1 Unknown 320 MG, EACH MORNING U U 0 320 MG QD
126576641 12657664 4 C SINVASTATINA SIMVASTATIN 1 Unknown UNK, EACH EVENING U U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126576641 12657664 1 Diabetes mellitus
126576641 12657664 3 Blood pressure management
126576641 12657664 4 Blood cholesterol

Outcome of event

Event ID CASEID OUTC COD
126576641 12657664 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126576641 12657664 Blood glucose increased
126576641 12657664 Eye haemorrhage
126576641 12657664 Underdose
126576641 12657664 Visual acuity reduced

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

no results found

Therapies reported

no results found