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
125737951 12573795 1 I 20160607 20160707 20160720 20160720 PER US-PFIZER INC-2016337159 PFIZER 48.00 YR M Y 0.00000 20160720 MD US US

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
125737951 12573795 1 PS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 UNK U 50670
125737951 12573795 2 SS CIPROFLOXACIN HCL CIPROFLOXACIN HYDROCHLORIDE 1 Intravenous (not otherwise specified) UNK U 77245 SOLUTION FOR INFUSION
125737951 12573795 3 C TOBRAMYCIN. TOBRAMYCIN 1 UNK 0
125737951 12573795 4 C FLUTICASONE W/SALMETEROL FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK 0
125737951 12573795 5 C MONTELUKAST MONTELUKAST SODIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125737951 12573795 2 Pseudomonas infection
125737951 12573795 3 Pseudomonas infection

Outcome of event

Event ID CASEID OUTC COD
125737951 12573795 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125737951 12573795 Electrocardiogram QT prolonged

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found