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
127606781 12760678 1 I 20151115 20160830 20160919 20160919 EXP PHHY2016IT119715 SANDOZ 41.64 YR F Y 0.00000 20160919 OT 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
127606781 12760678 1 PS CLARITHROMYCIN. CLARITHROMYCIN 1 Unknown Y 65136
127606781 12760678 2 SS PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Unknown Y 0
127606781 12760678 3 SS LEVOXACIN LEVOFLOXACIN 1 Unknown Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127606781 12760678 1 Helicobacter infection
127606781 12760678 2 Helicobacter infection
127606781 12760678 3 Helicobacter infection

Outcome of event

Event ID CASEID OUTC COD
127606781 12760678 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127606781 12760678 Dyspnoea
127606781 12760678 Erythema
127606781 12760678 Hypersensitivity
127606781 12760678 Palpitations

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
127606781 12760678 1 20151114 20151115 0
127606781 12760678 2 20151114 20151115 0
127606781 12760678 3 20151114 20151115 0