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
127352281 12735228 1 I 20160104 20160905 20160913 20160913 EXP GB-ORION CORPORATION ORION PHARMA-TREX2016-1697 ORION 34.00 YR F Y 86.00000 KG 20160913 MD 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
127352281 12735228 1 PS METHOTREXATE (TRADE NAME UNKNOWN) METHOTREXATE 1 Oral 0 15 MG
127352281 12735228 2 SS METHOTREXATE (TRADE NAME UNKNOWN) METHOTREXATE 1 Oral 0 25 MG /wk
127352281 12735228 3 SS ETANERCEPT ETANERCEPT 1 Subcutaneous 0 50 MG
127352281 12735228 4 SS FOLIC ACID. FOLIC ACID 1 Unknown 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127352281 12735228 3 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
127352281 12735228 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127352281 12735228 Headache
127352281 12735228 Photophobia
127352281 12735228 Vomiting

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
127352281 12735228 1 20150615 0
127352281 12735228 3 20150615 0
127352281 12735228 4 20150616 0