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
127363952 12736395 2 F 20151115 20160915 20160913 20160929 EXP IT-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-123365 RANBAXY 41.64 YR F Y 0.00000 20160929 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
127363952 12736395 1 SS CLARITHROMYCIN. CLARITHROMYCIN 1 Unknown UNK U U 0
127363952 12736395 2 PS Pantoprazole PANTOPRAZOLE SODIUM 1 Unknown UNK U U 200794
127363952 12736395 3 SS LEVOXACIN LEVOFLOXACIN 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127363952 12736395 1 Helicobacter infection
127363952 12736395 2 Helicobacter infection
127363952 12736395 3 Helicobacter infection

Outcome of event

Event ID CASEID OUTC COD
127363952 12736395 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127363952 12736395 Dyspnoea
127363952 12736395 Erythema
127363952 12736395 Hypersensitivity
127363952 12736395 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
127363952 12736395 1 20151114 20151115 0
127363952 12736395 2 20151114 20151115 0
127363952 12736395 3 20151114 20151115 0