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
126118041 12611804 1 I 20150101 20150925 20160801 20160801 PER US-PFIZER INC-3043877 PFIZER 62.00 YR F Y 0.00000 20160801 MD US US

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
126118041 12611804 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown U UNK 11719 SOLUTION FOR INJECTION
126118041 12611804 2 SS ETANERCEPT ETANERCEPT 1 Unknown UNK 0 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126118041 12611804 1 Product used for unknown indication
126118041 12611804 2 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126118041 12611804 Fatigue
126118041 12611804 Nausea
126118041 12611804 Pruritus generalised

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found