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
126906321 12690632 1 I 20160628 20160816 20160826 20160826 EXP IT-MINISAL02-371335 IT-TEVA-686542ACC TEVA 85.68 YR M Y 0.00000 20160826 MD IT IT

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
126906321 12690632 1 PS FUROSEMIDE. FUROSEMIDE 1 Oral 25 MILLIGRAM DAILY; U U 18413 25 MG TABLET
126906321 12690632 2 SS FUROSEMIDE. FUROSEMIDE 1 Oral 250 MILLIGRAM DAILY; U U 18413 250 MG TABLET
126906321 12690632 3 C ARANESP DARBEPOETIN ALFA 1 U 0
126906321 12690632 4 C ALLOPURINOL. ALLOPURINOL 1 Oral U 0 300 MG
126906321 12690632 5 C AMLODIPINE AMLODIPINE BESYLATE 1 Oral U 0
126906321 12690632 6 C RANITIDINE. RANITIDINE 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126906321 12690632 1 Product used for unknown indication
126906321 12690632 3 Product used for unknown indication
126906321 12690632 4 Product used for unknown indication
126906321 12690632 5 Product used for unknown indication
126906321 12690632 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126906321 12690632 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126906321 12690632 Dehydration
126906321 12690632 Orthostatic hypotension
126906321 12690632 Syncope

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
126906321 12690632 1 20160101 20160628 0
126906321 12690632 2 20160101 20160628 0