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
113597352 11359735 2 F 20160727 20150808 20160727 EXP TR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-051924 BRISTOL MYERS SQUIBB 65.00 YR M Y 0.00000 20160727 OT TR TR

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
113597352 11359735 1 PS METFORMIN HYDROCHLORIDE. METFORMIN HYDROCHLORIDE 1 Unknown 1000 MG, BID Y 20357 1000 MG BID
113597352 11359735 2 SS WARFARIN SODIUM. WARFARIN SODIUM 1 Unknown 5 MG, QD U 0 5 MG QD
113597352 11359735 3 C DILTIAZEM. DILTIAZEM 1 Unknown 90 MG, TID U 0 90 MG TID
113597352 11359735 4 C FLURBIPROFEN. FLURBIPROFEN 1 Unknown 100 MG, BID U 0 100 MG BID
113597352 11359735 5 C CLARITHROMYCIN. CLARITHROMYCIN 1 Unknown 500 MG, BID U 0 500 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113597352 11359735 1 Type 2 diabetes mellitus
113597352 11359735 2 Product used for unknown indication
113597352 11359735 3 Product used for unknown indication
113597352 11359735 4 Sinusitis
113597352 11359735 5 Sinusitis

Outcome of event

Event ID CASEID OUTC COD
113597352 11359735 HO
113597352 11359735 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113597352 11359735 Acute kidney injury
113597352 11359735 Haemoglobin decreased
113597352 11359735 International normalised ratio increased
113597352 11359735 Lactic acidosis
113597352 11359735 Platelet count increased
113597352 11359735 Urinary tract infection

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

no results found

Therapies reported

no results found