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
127868841 12786884 1 I 20160921 20160927 20160927 EXP DE-FRESENIUS KABI-FK201607117 FRESENIUS KABI AVRAM A,DUARTE C,PAPAGORAS C,RITIS K,JOSE SANTOS M,SCARPIONI R,ET AL.. IDENTIFYING PATIENT CANDIDATES FOR IL-1 INHIBITION:LESSONS FROM REAL-WORLD CASES. JOINT BONE SPINE 2015;ES17-ES29. 74.00 YR M Y 0.00000 20160927 MD DE DE

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
127868841 12786884 1 PS FUROSEMIDE (MANUFACTURER UNKNOWN) FUROSEMIDE 1 Unknown U U UNKNOWN 18902 75 MG UNKNOWN QD
127868841 12786884 2 I AMOXICILLIN (MANUFACTURER UNKNOWN) AMOXICILLIN 1 Unknown U U UNKNOWN 0 UNKNOWN
127868841 12786884 3 SS ALLOPURINOL. ALLOPURINOL 1 Unknown 0
127868841 12786884 4 C RAMIPRIL. RAMIPRIL 1 Unknown 0 5 MG QD
127868841 12786884 5 C METOPROLOL. METOPROLOL 1 Unknown 0 50 MG QD
127868841 12786884 6 C COLCHICINE. COLCHICINE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127868841 12786884 1 Diuretic therapy
127868841 12786884 2 Urinary tract infection
127868841 12786884 3 Gouty arthritis
127868841 12786884 4 Hypertension
127868841 12786884 5 Hypertension
127868841 12786884 6 Gouty arthritis

Outcome of event

Event ID CASEID OUTC COD
127868841 12786884 OT
127868841 12786884 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127868841 12786884 Abdominal pain
127868841 12786884 Blood potassium decreased
127868841 12786884 Dehydration
127868841 12786884 Dermatitis allergic
127868841 12786884 Diarrhoea
127868841 12786884 Drug hypersensitivity
127868841 12786884 Drug ineffective
127868841 12786884 Drug interaction
127868841 12786884 Gout
127868841 12786884 Hydronephrosis
127868841 12786884 Hypersensitivity vasculitis
127868841 12786884 Nausea
127868841 12786884 Nephrolithiasis
127868841 12786884 Urine output decreased
127868841 12786884 Vomiting
127868841 12786884 Weight decreased

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

no results found

Therapies reported

no results found