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
127647811 12764781 1 I 20150303 20151208 20160921 20160921 EXP JP-ROCHE-1690190 ROCHE 25.87 YR M Y 0.00000 20160921 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
127647811 12764781 1 PS Rituximab RITUXIMAB 1 Intravenous (not otherwise specified) 103705 500 MG SOLUTION FOR INFUSION
127647811 12764781 2 SS NEORAL CYCLOSPORINE 1 Unknown Y 0 50 MG
127647811 12764781 3 SS NEORAL CYCLOSPORINE 1 Unknown Y 0 50 MG
127647811 12764781 4 SS NEORAL CYCLOSPORINE 1 Unknown Y 0 100 MG
127647811 12764781 5 SS NEORAL CYCLOSPORINE 1 Unknown Y 0 75 MG
127647811 12764781 6 SS SULFAMETHOXAZOLE AND TRIMETHOPRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 1 TABLET (EVERY OTHER DAY) Y 0 TABLET
127647811 12764781 7 SS ZACRAS HD AMLODIPINE BESYLATEAZILSARTAN 1 Unknown U 0
127647811 12764781 8 C PREDNISOLONE. PREDNISOLONE 1 Oral 0 4 MG
127647811 12764781 9 C PREDNISOLONE. PREDNISOLONE 1 Oral 0 4 MG
127647811 12764781 10 C PREDNISOLONE. PREDNISOLONE 1 Oral 0 5 MG
127647811 12764781 11 C BREDININ MIZORIBINE 1 Oral 0 100 MG
127647811 12764781 12 C CALONAL ACETAMINOPHEN 1 Oral 0 400 MG
127647811 12764781 13 C NEOMALLERMIN-TR DEXCHLORPHENIRAMINE MALEATE 1 Oral 0 6 MG
127647811 12764781 14 C MICARDIS TELMISARTAN 1 Oral 0 40 MG
127647811 12764781 15 C FEBURIC FEBUXOSTAT 1 Oral 0 20 MG
127647811 12764781 16 C ATORVASTATIN ATORVASTATIN 1 Oral 0 10 MG
127647811 12764781 17 C BAKTAR SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 0 TABLET
127647811 12764781 18 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127647811 12764781 1 Nephrotic syndrome
127647811 12764781 2 Nephrotic syndrome
127647811 12764781 6 Infection prophylaxis
127647811 12764781 7 Product used for unknown indication
127647811 12764781 8 Nephrotic syndrome
127647811 12764781 11 Nephrotic syndrome
127647811 12764781 12 Premedication
127647811 12764781 13 Premedication
127647811 12764781 14 Hypertension
127647811 12764781 15 Hyperuricaemia
127647811 12764781 16 Dyslipidaemia

Outcome of event

Event ID CASEID OUTC COD
127647811 12764781 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127647811 12764781 Hyperkalaemia
127647811 12764781 Infusion related reaction
127647811 12764781 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
127647811 12764781 1 20150303 20151127 0
127647811 12764781 2 20110719 20150723 0
127647811 12764781 3 20151211 20160128 0
127647811 12764781 4 20160129 20160303 0
127647811 12764781 5 20160304 20160630 0
127647811 12764781 6 20160630 0
127647811 12764781 8 20110319 20151203 0
127647811 12764781 9 20160323 0
127647811 12764781 10 20160324 0
127647811 12764781 11 20140925 20141023 0
127647811 12764781 12 20150303 20151127 0
127647811 12764781 13 20150303 20151127 0
127647811 12764781 14 20151203 0
127647811 12764781 15 20151203 0
127647811 12764781 16 20151203 0
127647811 12764781 17 20160630 0