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
125020923 12502092 3 F 20160614 20160711 20160627 20160712 PER IT-SA-2016SA113485 AVENTIS 0.00 A M Y 0.00000 20160712 CN 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
125020923 12502092 1 SS SOLOSTAR DEVICE 1 U BF423A 0 TID
125020923 12502092 2 PS APIDRA SOLOSTAR INSULIN GLULISINE 1 Subcutaneous 6-10-8 IU U BF423A 21629 SOLUTION FOR INJECTION TID
125020923 12502092 3 C LASIX FUROSEMIDE 1 MORNING-LUNCH 0
125020923 12502092 4 C CARDICOR BISOPROLOL 1 MORNING 0
125020923 12502092 5 C ANTRA OMEPRAZOLE 1 MORNING 0
125020923 12502092 6 C DELTACORTENE PREDNISONE 1 MORNING 0
125020923 12502092 7 C CARDIOASPIRINA ASPIRIN 1 LUNCH 0
125020923 12502092 8 C FERROUS SULFATE. FERROUS SULFATE 1 LUNCH 0
125020923 12502092 9 C FOLINA FOLIC ACID 1 0
125020923 12502092 10 C LUVION CANRENONE 1 0
125020923 12502092 11 C PLAVIX CLOPIDOGREL BISULFATE 1 EVENING 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125020923 12502092 1 Diabetes mellitus
125020923 12502092 2 Diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125020923 12502092 Device issue
125020923 12502092 Hyperglycaemia
125020923 12502092 Muscular weakness
125020923 12502092 Pain in extremity

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

no results found

Therapies reported

no results found