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
124654383 12465438 3 F 20160414 20160624 20160614 20160705 EXP US-SA-2016SA110868 AVENTIS 76.00 YR E F Y 0.00000 20160705 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
124654383 12465438 1 PS APIDRA INSULIN GLULISINE 1 Unknown DOSE:40 UNIT(S) 5F440A 21629 SOLUTION FOR INJECTION QD
124654383 12465438 2 SS APIDRA INSULIN GLULISINE 1 Unknown DOSE:40 UNIT(S) 5F441A 21629 SOLUTION FOR INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124654383 12465438 1 Type 1 diabetes mellitus
124654383 12465438 2 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124654383 12465438 HO
124654383 12465438 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124654383 12465438 Atrial fibrillation
124654383 12465438 Blood glucose increased
124654383 12465438 Drug ineffective
124654383 12465438 Heart rate increased
124654383 12465438 Hypertension
124654383 12465438 Pulmonary fibrosis
124654383 12465438 Pulmonary hypertension
124654383 12465438 Wrong technique in product usage process

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
124654383 12465438 1 2006 0
124654383 12465438 2 2006 0