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
5374429 5801347 I 5374429-1 20050422 20070618 20070629 EXP JP-JNJFOC-20050502674 CENTOCOR PHARMACOVIGILANCE F Y 64 KG 20070629 MD 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
5374429 1008645904 SS REMICADE 1 INTRAVENOUS
5374429 1008645905 SS REMICADE 1 INTRAVENOUS
5374429 1008645906 PS REMICADE 1 INTRAVENOUS
5374429 1008645907 C RHEUMATREX 1 ORAL
5374429 1008645908 C RHEUMATREX 1 ORAL
5374429 1008645909 C LOXONIN 2 ORAL
5374429 1008645911 C LOXONIN 2 ORAL 2T
5374429 1008645912 C LEUCOVORIN CALCIUM 1 ORAL 1T
5374429 1008645913 C TAKEPRON 2 ORAL
5374429 1008645914 C NORVASC 1 ORAL
5374429 1008645915 C PREDONINE 2 ORAL
5374429 1008645916 C ADRENAL HORMONE PREPARATIONS 2
5374429 1008645917 C TAKEPRON 2
5374429 1008645918 C LOXONIN 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5374429 1008645906 RHEUMATOID ARTHRITIS
5374429 1008645908 RHEUMATOID ARTHRITIS
5374429 1008645911 RHEUMATOID ARTHRITIS
5374429 1008645912 RHEUMATOID ARTHRITIS
5374429 1008645915 RHEUMATOID ARTHRITIS
5374429 1008645916 RHEUMATOID ARTHRITIS

Outcome of event

Event ID OUTC COD
5374429 HO
5374429 OT

Reactions reported

Event ID PT
5374429 ARTHRALGIA
5374429 LYMPH NODE TUBERCULOSIS

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5374429 1008645907 20011201
5374429 1008645908 20011201
5374429 1008645912 20011201
5374429 1008645917 20040312