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
126735291 12673529 1 I 20160805 20160812 20160822 20160822 EXP PHHY2016IT114250 SANDOZ 90.84 YR M Y 0.00000 20160822 OT 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
126735291 12673529 1 PS ACETYLSALICYLIC ACID ASPIRIN 1 Oral 1 DF, QD 218 DF 0 1 DF TABLET QD
126735291 12673529 2 SS ARIXTRA FONDAPARINUX SODIUM 1 Subcutaneous 1 DF, QD 218 DF 0 1 DF SOLUTION FOR INJECTION QD
126735291 12673529 3 C LASIX FUROSEMIDE 1 Oral U 0
126735291 12673529 4 C LANSOX LANSOPRAZOLE 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126735291 12673529 1 Thrombosis prophylaxis
126735291 12673529 2 Thrombosis prophylaxis
126735291 12673529 3 Product used for unknown indication
126735291 12673529 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126735291 12673529 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126735291 12673529 Gastrointestinal haemorrhage
126735291 12673529 Haematemesis
126735291 12673529 Loss of consciousness

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
126735291 12673529 1 20160101 20160805 0
126735291 12673529 2 20160101 20160805 0