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
123423622 12342362 2 F 2015 20160719 20160506 20160727 EXP GB-PFIZER INC-2016237946 PFIZER 61.00 YR M Y 105.00000 KG 20160727 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
123423622 12342362 1 PS AMLODIPINE BESILATE AMLODIPINE BESYLATE 1 UNK Y 19787
123423622 12342362 2 SS INDAPAMIDE. INDAPAMIDE 1 Unknown UNK 80 MG Y 0
123423622 12342362 3 C DOXAZOSIN MESILATE DOXAZOSIN MESYLATE 1 Unknown UNK 0
123423622 12342362 4 C FUROSEMIDE. FUROSEMIDE 1 20 MG, BID 0 20 MG BID
123423622 12342362 5 C FUROSEMIDE. FUROSEMIDE 1 Unknown 60 UNK, 20 MG IN MORNING, 40 MG IN EVENING 0 60 MG
123423622 12342362 6 C RAMIPRIL. RAMIPRIL 1 UNK 0
123423622 12342362 7 C REGURIN 2 UNK 0
123423622 12342362 8 C VALSARTAN. VALSARTAN 1 80 MG, QD 0 80 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123423622 12342362 1 Hypertension
123423622 12342362 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
123423622 12342362 LT
123423622 12342362 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123423622 12342362 Glomerular filtration rate decreased
123423622 12342362 Oedema peripheral

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
123423622 12342362 1 2015 2015 0
123423622 12342362 2 20141030 2015 0
123423622 12342362 5 20160215 20160309 0