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
126822631 12682263 1 I 20160817 20160824 20160824 EXP PHHY2016CH115602 SANDOZ 68.00 YR F Y 0.00000 20160825 OT CH CH

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
126822631 12682263 1 PS AZITHROMYCIN ANHYDROUS. AZITHROMYCIN ANHYDROUS 1 Oral 250 MG/3X PER WEEK U 65209 250 MG
126822631 12682263 2 I CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, QD U 0 500 MG QD
126822631 12682263 3 I CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 10 MG, QD U 0 10 MG QD
126822631 12682263 4 I DOMPERIDONE DOMPERIDONE 1 Oral 30 MG, QD U 0 30 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126822631 12682263 1 Product used for unknown indication
126822631 12682263 2 Product used for unknown indication
126822631 12682263 3 Product used for unknown indication
126822631 12682263 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126822631 12682263 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126822631 12682263 Cardiomyopathy
126822631 12682263 Drug interaction
126822631 12682263 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