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
121928185 12192818 5 F 201508 20160825 20160318 20160901 EXP CA-PFIZER INC-2016162051 PFIZER 68.00 YR F Y 0.00000 20160901 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
121928185 12192818 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 2.5 MG, WEEKLY INJECTION 11719 2.5 MG SOLUTION FOR INJECTION /wk
121928185 12192818 2 SS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 203214 5 MG TABLET BID
121928185 12192818 3 SS CELEBREX CELECOXIB 1 UNK 20998 CAPSULE, HARD
121928185 12192818 4 SS ACTEMRA TOCILIZUMAB 1 UNK N 0
121928185 12192818 5 SS TYLENOL WITH CODEINE ACETAMINOPHENCODEINE PHOSPHATE 1 UNK, AS NEEDED 0
121928185 12192818 6 SS PREDNISONE. PREDNISONE 1 2.5 MG N 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121928185 12192818 1 Rheumatoid arthritis
121928185 12192818 2 Rheumatoid arthritis
121928185 12192818 3 Rheumatoid arthritis
121928185 12192818 4 Rheumatoid arthritis
121928185 12192818 5 Pain

Outcome of event

Event ID CASEID OUTC COD
121928185 12192818 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121928185 12192818 Arthralgia
121928185 12192818 Constipation
121928185 12192818 Emphysema
121928185 12192818 Hypoaesthesia
121928185 12192818 Lung infection
121928185 12192818 Pain
121928185 12192818 Tuberculosis

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
121928185 12192818 2 20160401 0
121928185 12192818 4 20160304 0