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
127104341 12710434 1 I 20160606 20160825 20160902 20160902 EXP JP-AMGEN-JPNCT2016116324 AMGEN 64.00 YR A M Y 45.00000 KG 20160902 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
127104341 12710434 1 PS darbepoetin alfa DARBEPOETIN ALFA 1 Subcutaneous 60 MUG, Q4WK 103951 60 UG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
127104341 12710434 2 SS darbepoetin alfa DARBEPOETIN ALFA 1 Subcutaneous 60 MUG, UNK 103951 60 UG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
127104341 12710434 3 SS darbepoetin alfa DARBEPOETIN ALFA 1 Subcutaneous 90 MUG, UNK 103951 90 UG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
127104341 12710434 4 SS darbepoetin alfa DARBEPOETIN ALFA 1 Subcutaneous 120 MUG, Q4WK 103951 120 UG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
127104341 12710434 5 SS AMLODIPINE AMLODIPINE BESYLATE 1 Oral 5 MG, BID 0 5 MG BID
127104341 12710434 6 SS KAYEXALATE SODIUM POLYSTYRENE SULFONATE 1 Oral 3.27 G, BID 0 3.27 G SYRUP BID
127104341 12710434 7 SS SODIUM BICARBONATE. SODIUM BICARBONATE 1 Unknown 5 G, BID 0 5 G BID
127104341 12710434 8 SS ALLOPURINOL. ALLOPURINOL 1 Oral 50 MG, QD 0 50 MG TABLET QD
127104341 12710434 9 SS CALFINA ALFACALCIDOL 1 Oral 0.25 MUG, QD 0 .25 UG TABLET QD
127104341 12710434 10 SS ARTIST CARVEDILOL 1 Oral 5 MG, QD 0 5 MG TABLET QD
127104341 12710434 11 SS FUROSEMIDE. FUROSEMIDE 1 Oral 20 MG, QD 0 20 MG TABLET QD
127104341 12710434 12 SS CALTAN CALCIUM CARBONATE 1 Oral 1000 MG, TID 0 1000 MG TID
127104341 12710434 13 SS ZONISAMIDE. ZONISAMIDE 1 Oral 100 MG, BID 0 100 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127104341 12710434 1 Chronic kidney disease
127104341 12710434 5 Hypertension
127104341 12710434 6 Hyperkalaemia
127104341 12710434 7 Acidosis
127104341 12710434 8 Hyperuricaemia
127104341 12710434 9 Hyperparathyroidism secondary
127104341 12710434 10 Hypertension
127104341 12710434 11 Hypertension
127104341 12710434 12 Hyperphosphataemia
127104341 12710434 13 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
127104341 12710434 DS
127104341 12710434 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127104341 12710434 Gout
127104341 12710434 Haemodialysis
127104341 12710434 Renal impairment

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
127104341 12710434 1 20150805 0
127104341 12710434 2 20151230 0
127104341 12710434 3 20160127 0
127104341 12710434 4 20160224 0
127104341 12710434 5 20150513 0
127104341 12710434 6 20130612 0
127104341 12710434 7 20150613 0
127104341 12710434 8 20160513 0
127104341 12710434 9 20151230 0
127104341 12710434 10 20160224 0
127104341 12710434 11 20160513 0
127104341 12710434 12 20160513 0
127104341 12710434 13 2003 0