The Safety Rates Drug Report

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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
6661217 7339072 I 6661217-9 20090730 20100323 20100331 EXP JP-ROCHE-694025 ROCHE 83 M Y 50 KG 20100331 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
6661217 1013420005 PS TOCILIZUMAB 2 INTRAVENOUS DRIP
6661217 1013420006 SS REMICADE 1 ORAL DOSE FORM: PERORAL AGENT
6661217 1013420007 C METHOTREXATE 1 ORAL DOSE FORM: PERORAL AGENT
6661217 1013420008 C PREDNISOLONE 1 ORAL DOSE FORM: PERORAL AGENT
6661217 1013420009 C LANSOPRAZOLE 1 ORAL
6661217 1013420010 C LIPITOR 1 ORAL
6661217 1013420011 C EUGLUCON 2 ORAL
6661217 1013420012 C FOLIC ACID 1 ORAL
6661217 1013420013 C MAGMITT 2 ORAL
6661217 1013420014 C PRORENAL 2 ORAL
6661217 1013420015 C FLIVAS 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6661217 1013420005 RHEUMATOID ARTHRITIS
6661217 1013420006 RHEUMATOID ARTHRITIS

Outcome of event

Event ID OUTC COD
6661217 HO

Reactions reported

Event ID PT
6661217 BLADDER CANCER

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
6661217 1013420005 20090723 20090723
6661217 1013420006 20080709 20090528