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
127028091 12702809 1 I 20160808 20160829 20160831 20160831 EXP GB-MHRA-TPP23271402C2389067YC1471603194534 GB-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-071186 BRISTOL MYERS SQUIBB 76.00 YR M Y 88.00000 KG 20160831 CN GB GB

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
127028091 12702809 1 PS ELIQUIS APIXABAN 1 Unknown U U 202155 FILM-COATED TABLET
127028091 12702809 2 SS ASPIRIN. ASPIRIN 1 Unknown 1 DF, UNK U 0 1 DF
127028091 12702809 3 SS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Unknown 1 DF, QD 60 DF U 0 1 DF QD
127028091 12702809 4 C ATORVASTATIN ATORVASTATIN 1 Unknown 1 DF, QD 18 DF U 0 1 DF QD
127028091 12702809 5 C BISOPROLOL BISOPROLOL 1 Unknown 1 DF, BID 894 DF U 0 1 DF BID
127028091 12702809 6 C FELODIPINE. FELODIPINE 1 Unknown 1 DF, QD 18 DF U 0 1 DF QD
127028091 12702809 7 C FUROSEMIDE. FUROSEMIDE 1 Unknown 1 DF, QD 60 DF U 0 1 DF QD
127028091 12702809 8 C GLICLAZIDE GLICLAZIDE 1 Unknown 1 DF, QD 213.899994 DF U 0 1 DF QD
127028091 12702809 9 C OMEPRAZOLE. OMEPRAZOLE 1 Unknown 1 DF, QD 11 DF U 0 1 DF QD
127028091 12702809 10 C RAMIPRIL. RAMIPRIL 1 Unknown 1 DF, QD 18 DF U 0 1 DF QD
127028091 12702809 11 C ROSUVASTATIN. ROSUVASTATIN 1 Unknown 1 DF, QWK 1.5 DF U 0 1 DF /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127028091 12702809 1 Cerebrovascular accident prophylaxis
127028091 12702809 2 Product used for unknown indication
127028091 12702809 3 Product used for unknown indication
127028091 12702809 4 Product used for unknown indication
127028091 12702809 5 Product used for unknown indication
127028091 12702809 6 Product used for unknown indication
127028091 12702809 7 Oedema
127028091 12702809 8 Diabetes mellitus
127028091 12702809 9 Prophylaxis
127028091 12702809 10 Product used for unknown indication
127028091 12702809 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127028091 12702809 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127028091 12702809 Contraindicated product administered
127028091 12702809 Dyspepsia
127028091 12702809 Gastrointestinal haemorrhage
127028091 12702809 Rectal haemorrhage

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
127028091 12702809 1 20160725 0
127028091 12702809 2 20160609 20160804 0
127028091 12702809 3 20160609 0
127028091 12702809 4 20160721 20160819 0
127028091 12702809 5 20150519 0
127028091 12702809 6 20160721 0
127028091 12702809 7 20160609 20160707 0
127028091 12702809 8 20160107 0
127028091 12702809 9 20160819 0
127028091 12702809 10 20160721 0
127028091 12702809 11 20160819 0