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
126298621 12629862 1 I 20150518 20160728 20160808 20160808 EXP IT-SA-2016SA140069 AVENTIS 74.00 YR E M Y 0.00000 20160808 PH IT IT

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
126298621 12629862 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Subcutaneous DOSE-20 IU,IN THOUSANDS DAILY U U 21081 SOLUTION FOR INJECTION QD
126298621 12629862 2 SS HUMALOG INSULIN LISPRO 1 Subcutaneous DOSE-19 IU,IN THOUSANDS U U 0 SOLUTION FOR INJECTION QD
126298621 12629862 3 C PANTORC PANTOPRAZOLE SODIUM 1 STRENGTH: 40 MG 0 GASTRO-RESISTANT TABLET
126298621 12629862 4 C LASIX FUROSEMIDE 1 STRENGTH: 25 MG 0 TABLET
126298621 12629862 5 C STILNOX ZOLPIDEM TARTRATE 1 STRENGTH: 10 MG 0 FILM-COATED TABLET
126298621 12629862 6 C CARDIOASPIRIN ASPIRIN 1 STRENGTH: 100 MG 0 GASTRO-RESISTANT TABLET
126298621 12629862 7 C FLUXUM PARNAPARIN SODIUM 1 Subcutaneous DOSE: 3.200 I.U 0
126298621 12629862 8 C SOLOSTAR DEVICE 1 0 QD
126298621 12629862 9 C KWIKPEN 2 Subcutaneous 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126298621 12629862 1 Diabetes mellitus
126298621 12629862 8 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126298621 12629862 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126298621 12629862 Compensatory sweating
126298621 12629862 Hypoglycaemia

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

no results found

Therapies reported

no results found