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
127552261 12755226 1 I 20160525 20160907 20160916 20160916 EXP GB-TEVA-692589ACC TEVA 48.00 YR M Y 70.00000 KG 20160916 OT GB GB

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
127552261 12755226 1 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Subcutaneous 3453.57142 MG U U UNK 0 25 MG /wk
127552261 12755226 2 PS PREDNISOLONE. PREDNISOLONE 1 Unknown 10 MILLIGRAM DAILY; 1569.58333 MG U UNK 89081 10 MG INJECTION QD
127552261 12755226 3 SS PREDNISOLONE. PREDNISOLONE 1 Unknown 20 MILLIGRAM DAILY; 1569.58333 MG U UNK 89081 20 MG QD
127552261 12755226 4 SS ETANERCEPT ETANERCEPT 1 Intradermal 14.2797619 MG D U UNK 0 1 MG INJECTION /wk
127552261 12755226 5 C FOLIC ACID. FOLIC ACID 1 Oral 6 DAYS A WEEK 0 5 MG
127552261 12755226 6 C ORAMORPH MORPHINE SULFATE 1 Oral 0 5 MG SUPPOSITORY
127552261 12755226 7 C VOLTAROL DICLOFENAC SODIUM 1 Rectal 400 MG 0 50 MG SUPPOSITORY BID

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127552261 12755226 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127552261 12755226 Sepsis

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
127552261 12755226 1 20131001 0
127552261 12755226 2 20151220 0
127552261 12755226 4 20160215 20160510 0
127552261 12755226 5 20131001 0
127552261 12755226 6 20160521 0
127552261 12755226 7 20160521 20160523 0