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
126486021 12648602 1 I 20160705 20160805 20160812 20160812 EXP PHHY2016PH109564 SANDOZ 0.00 M Y 0.00000 20160812 OT PH PH

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
126486021 12648602 1 PS VANCOMYCIN VANCOMYCIN 1 Intravenous (not otherwise specified) 1.5 G, Q12H U 90250 1.5 G INJECTION Q12H
126486021 12648602 2 SS VANCOMYCIN VANCOMYCIN 1 Intravenous (not otherwise specified) 1 G, Q8H U 90250 1 G INJECTION Q8H
126486021 12648602 3 SS VANCOMYCIN VANCOMYCIN 1 Intravenous (not otherwise specified) 1.25 G, Q12H U 90250 1.25 G INJECTION Q12H
126486021 12648602 4 SS VANCOMYCIN VANCOMYCIN 1 Intravenous (not otherwise specified) 1 G, Q12H U 90250 1 G INJECTION Q12H

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126486021 12648602 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126486021 12648602 Disease progression
126486021 12648602 Hypersensitivity
126486021 12648602 Rash
126486021 12648602 Rash morbilliform
126486021 12648602 Red man syndrome

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
126486021 12648602 1 20160627 0