The Safety Rates Drug Report

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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
115380004 11538000 4 F 20150903 20160824 20150922 20160824 EXP JP-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-061860 BRISTOL MYERS SQUIBB 63.08 YR M Y 75.00000 KG 20160824 MD JP JP

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
115380004 11538000 1 PS ELIQUIS APIXABAN 1 Oral 5 MG, BID 650.942993 MG 202155 5 MG FILM-COATED TABLET BID
115380004 11538000 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral 75 MG, QD 825 MG 0 75 MG QD
115380004 11538000 3 C MAINTATE BISOPROLOL FUMARATE 1 Oral 25 MG, QD U 0 25 MG QD
115380004 11538000 4 C LASIX FUROSEMIDE 1 Oral 40 MG, BID U 0 40 MG BID
115380004 11538000 5 C FLUITRAN TRICHLORMETHIAZIDE 1 Oral 2 MG, QD U 0 2 MG QD
115380004 11538000 6 C FLUITRAN TRICHLORMETHIAZIDE 1 Oral 5 UNK, UNK U 0 5 MG QD
115380004 11538000 7 C SELARA EPLERENONE 1 Oral 50 MG, QD U 0 50 MG QD
115380004 11538000 8 C TRAZENTA LINAGLIPTIN 1 Oral 5 MG, UNK U 0 5 MG QD
115380004 11538000 9 C ARTIST CARVEDILOL 1 Oral 2.5 MG, UNK U 0 2.5 MG BID
115380004 11538000 10 C AMARYL GLIMEPIRIDE 1 Oral 1 MG, UNK U 0 1 MG QD
115380004 11538000 11 C LUPRAC TORSEMIDE 1 Oral 4 MG, UNK U 0 4 MG QD
115380004 11538000 12 C COVERSYL /00790702/ PERINDOPRIL 1 Oral 4 MG, UNK U 0 4 MG QD
115380004 11538000 13 C FEBURIC FEBUXOSTAT 1 Oral 20 MG, UNK U 0 20 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115380004 11538000 1 Cerebrovascular accident prophylaxis
115380004 11538000 2 Thrombosis prophylaxis
115380004 11538000 3 Product used for unknown indication
115380004 11538000 4 Product used for unknown indication
115380004 11538000 5 Product used for unknown indication
115380004 11538000 7 Product used for unknown indication
115380004 11538000 8 Product used for unknown indication
115380004 11538000 9 Product used for unknown indication
115380004 11538000 10 Product used for unknown indication
115380004 11538000 11 Product used for unknown indication
115380004 11538000 12 Product used for unknown indication
115380004 11538000 13 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
115380004 11538000 DE
115380004 11538000 DS
115380004 11538000 HO
115380004 11538000 LT
115380004 11538000 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115380004 11538000 Cerebral haemorrhage
115380004 11538000 Contraindicated product administered
115380004 11538000 Meningitis bacterial
115380004 11538000 Pneumonia
115380004 11538000 Sinusitis

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
115380004 11538000 1 20150716 20150906 0
115380004 11538000 2 20150827 20150906 0