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
126084881 12608488 1 I 20160702 20160714 20160729 20160729 EXP PK-SA-2016SA131584 AVENTIS 50.00 YR A F Y 0.00000 20160729 CN PK PK

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
126084881 12608488 1 PS LANTUS INSULIN GLARGINE 1 Subcutaneous DOSE:36 UNIT(S) 5F233A 21081 INJECTION QD
126084881 12608488 2 SS APIDRA INSULIN GLULISINE 1 Subcutaneous 20+20+20UNIT?S/TDS DOSE:20 UNIT(S) 5F009A 21629 INJECTION TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126084881 12608488 1 Blood glucose abnormal
126084881 12608488 2 Blood glucose abnormal

Outcome of event

Event ID CASEID OUTC COD
126084881 12608488 HO
126084881 12608488 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126084881 12608488 Blood glucose increased
126084881 12608488 Cardiopulmonary failure
126084881 12608488 Headache
126084881 12608488 Polyuria
126084881 12608488 Pyrexia
126084881 12608488 Somnolence

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
126084881 12608488 1 20160702 20160724 0
126084881 12608488 2 20160702 20160724 0