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
127643531 12764353 1 I 2010 20160908 20160920 20160920 EXP GB-TEVA-692705ACC TEVA 75.00 YR F Y 0.00000 20160921 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
127643531 12764353 1 PS BISOPROLOL FUMARATE. BISOPROLOL FUMARATE 1 2.5 MILLIGRAM DAILY; Y U 19982 2.5 MG TABLET QD
127643531 12764353 2 SS BISOPROLOL FUMARATE. BISOPROLOL FUMARATE 1 .5 DOSAGE FORMS DAILY; Y U 19982 .5 DF TABLET QD
127643531 12764353 3 C ALENDRONIC ACID ALENDRONIC ACID 1 0
127643531 12764353 4 C ATORVASTATIN ATORVASTATIN 1 0
127643531 12764353 5 C CANDESARTAN CANDESARTAN 1 0
127643531 12764353 6 C FUROSEMIDE. FUROSEMIDE 1 0
127643531 12764353 7 C WARFARIN WARFARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127643531 12764353 1 Cardiac disorder

Outcome of event

Event ID CASEID OUTC COD
127643531 12764353 DE
127643531 12764353 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127643531 12764353 Death
127643531 12764353 Leukaemia
127643531 12764353 Off label use
127643531 12764353 Pain in extremity
127643531 12764353 Peripheral coldness
127643531 12764353 Peripheral swelling
127643531 12764353 Skin discolouration

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
127643531 12764353 1 2006 2010 0
127643531 12764353 2 2010 2011 0