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
126118121 12611812 1 I 20150901 20150923 20160801 20160801 PER US-PFIZER INC-3029528 PFIZER 45.00 YR F Y 0.00000 20160801 OT 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
126118121 12611812 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Other INJECTION U UNK 11719 SOLUTION FOR INJECTION
126118121 12611812 2 SS ETANERCEPT ETANERCEPT 1 Other 50 MG, INJECTION, FREQ: 1 WEEK; INTERVAL: 1 U 0 50 MG SOLUTION FOR INJECTION
126118121 12611812 3 C ADALIMUMAB ADALIMUMAB 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126118121 12611812 1 Product used for unknown indication
126118121 12611812 2 Rheumatoid arthritis
126118121 12611812 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126118121 12611812 Abdominal pain
126118121 12611812 Fatigue
126118121 12611812 Feeling abnormal
126118121 12611812 Head discomfort
126118121 12611812 Headache
126118121 12611812 Malaise
126118121 12611812 Myalgia
126118121 12611812 Somnolence

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
126118121 12611812 1 20150904 0
126118121 12611812 2 20150904 0