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
126293401 12629340 1 I 20150827 20160726 20160808 20160808 EXP IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-061885 BRISTOL MYERS SQUIBB 75.46 YR F Y 0.00000 20160808 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
126293401 12629340 1 PS COUMADIN WARFARIN SODIUM 1 Oral 5 MG, QD U 9218 5 MG TABLET QD
126293401 12629340 2 C BISOPROLOL /00802602/ BISOPROLOL 1 Unknown UNK, QD U 0 QD
126293401 12629340 3 C FUROSEMIDE. FUROSEMIDE 1 Unknown 25 MG, UNK U 0 25 MG
126293401 12629340 4 C LUVION /00252501/ CANRENONE 1 Unknown 50MG QD U 0 50 MG CAPSULE QD
126293401 12629340 5 C ALLOPURINOL. ALLOPURINOL 1 Unknown 300 MG, QD U 0 300 MG CAPSULE QD
126293401 12629340 6 C FOLINA /00024201/ FOLIC ACID 1 Unknown 1 DF, QD U 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126293401 12629340 1 Valvuloplasty cardiac
126293401 12629340 2 Product used for unknown indication
126293401 12629340 3 Product used for unknown indication
126293401 12629340 4 Product used for unknown indication
126293401 12629340 5 Product used for unknown indication
126293401 12629340 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126293401 12629340 OT
126293401 12629340 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126293401 12629340 Asthenia
126293401 12629340 Diarrhoea haemorrhagic
126293401 12629340 International normalised ratio increased
126293401 12629340 Vomiting

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

no results found

Therapies reported

no results found