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
125221301 12522130 1 I 20160623 20160701 20160701 EXP US-SA-2016SA120174 AVENTIS 0.00 A F Y 0.00000 20160701 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
125221301 12522130 1 PS LANTUS INSULIN GLARGINE 1 Unknown UNKNOWN 21081
125221301 12522130 2 SS NOVOLOG INSULIN ASPART 1 Unknown U UNK 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125221301 12522130 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125221301 12522130 Blood glucose increased
125221301 12522130 Memory impairment
125221301 12522130 Somnolence
125221301 12522130 Treatment noncompliance
125221301 12522130 Viral infection

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

no results found

Therapies reported

no results found