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
125538971 12553897 1 I 20160629 20160713 20160713 EXP CA-HQ SPECIALTY-CA-2016INT000517 INTERCHEM 45.00 YR F Y 0.00000 20160713 CN CA CA

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
125538971 12553897 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral UNK 201749
125538971 12553897 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK 201749
125538971 12553897 3 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown UNK 0
125538971 12553897 4 SS NAPROXEN. NAPROXEN 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125538971 12553897 1 Rheumatoid arthritis
125538971 12553897 3 Product used for unknown indication
125538971 12553897 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125538971 12553897 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125538971 12553897 Drug hypersensitivity
125538971 12553897 Fall
125538971 12553897 Nausea
125538971 12553897 Weight increased

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
125538971 12553897 2 2013 201604 0
125538971 12553897 3 201605 0