The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6527774 7178631 F 5 6527774-8 20091021 20091218 20091231 EXP 8053795 UCB, INC., 30 F N 20091230 JAPAN

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6527774 1012904013 PS CERTOLIZUMAB PEGOL (CERTOLIZUMAB PEGOL) 2 Y
6527774 1012951951 C METHOTREXATE 1
6527774 1012951952 C FOLIC ACID 1
6527774 1012951953 C MELOXICAM 2
6527774 1012951954 C PREDNISOLONE 1
6527774 1012951956 C LOXOPROFEN SODIUM 2
6527774 1012951957 C INDOMETHACIN 1
6527774 1012951958 C CLARITHROMYCIN 2
6527774 1012951959 C TEPRENONE 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6527774 1012904013 RHEUMATOID ARTHRITIS

Outcome of event

Event ID OUTC COD
6527774 HO

Reactions reported

Event ID PT
6527774 ANIMAL BITE
6527774 FEELING HOT
6527774 INFECTIVE TENOSYNOVITIS
6527774 PAIN IN EXTREMITY
6527774 STAPHYLOCOCCAL INFECTION
6527774 SWELLING

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

Event ID RPSR COD
6527774 FGN
6527774 HP
6527774 OTH
6527774 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6527774 1012904013 20090826 20091021
6527774 1012904013 20090511