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
126100241 12610024 1 I 20160628 20160727 20160801 20160801 EXP FR-009507513-1607FRA012323 MERCK 50.81 YR M Y 0.00000 20160801 OT FR FR

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
126100241 12610024 1 SS POLARAMINE DEXCHLORPHENIRAMINE MALEATE 1 Intravenous (not otherwise specified) 5 MG, UNK 0 5 MG INJECTION
126100241 12610024 2 SS ERBITUX CETUXIMAB 1 Intravenous (not otherwise specified) 555 MG, UNK Y 0 555 MG
126100241 12610024 3 PS HYDROCORTISONE. HYDROCORTISONE 1 Intravenous (not otherwise specified) 100 MG, UNK 8506 100 MG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126100241 12610024 1 Allergy prophylaxis
126100241 12610024 2 Colorectal cancer
126100241 12610024 3 Prophylaxis of nausea and vomiting

Outcome of event

Event ID CASEID OUTC COD
126100241 12610024 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126100241 12610024 Erythema
126100241 12610024 Hypersensitivity
126100241 12610024 Hypotension
126100241 12610024 Pruritus

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
126100241 12610024 1 20160628 0
126100241 12610024 2 20160628 20160628 0
126100241 12610024 3 20160628 0