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
127772531 12777253 1 I 20160606 20160915 20160924 20160924 EXP GB-MHRA-ADR 23642231 GB-ACCORD-044225 ACCORD 0.00 F Y 0.00000 20160924 PH 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
127772531 12777253 1 PS LISINOPRIL. LISINOPRIL 1 Oral Y 202554 20 MG QD
127772531 12777253 2 SS DIGOXIN. DIGOXIN 1 Oral IN THE MORNING Y 0 250 UG QD
127772531 12777253 3 C AMLODIPINE AMLODIPINE BESYLATE 1 0
127772531 12777253 4 C FOSTAIR BECLOMETHASONEFORMOTEROL 1 0
127772531 12777253 5 C FUROSEMIDE. FUROSEMIDE 1 0
127772531 12777253 6 C IBANDRONIC ACID IBANDRONIC ACID 1 0
127772531 12777253 7 C LEFLUNOMIDE. LEFLUNOMIDE 1 0
127772531 12777253 8 C OMEPRAZOLE. OMEPRAZOLE 1 0
127772531 12777253 9 C TIOTROPIUM TIOTROPIUM 1 0
127772531 12777253 10 C WARFARIN WARFARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127772531 12777253 1 Hypertension
127772531 12777253 2 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
127772531 12777253 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127772531 12777253 Acute kidney injury
127772531 12777253 Decreased appetite
127772531 12777253 Fluid intake reduced
127772531 12777253 Hyperkalaemia
127772531 12777253 Toxicity to various agents

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
127772531 12777253 1 20160607 0
127772531 12777253 2 20160607 0