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
7583762 8017035 I 7583762-4 20110621 20110622 20110630 EXP AR-ROCHE-785465 ROCHE 62 YR M Y 167 KG 20110630 MD ARGENTINA

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
7583762 1016905419 PS TOCILIZUMAB 2 INTRAVENOUS FREQUENCY Q4S, LAST DOSE PRIOR TO SAE ON 02 JUNE 2010. TOTAL MONTHLY DOSE: 656 MG. B007
7583762 1016905422 C PREDNISONE 1 ORAL
7583762 1016905421 C PREDNISONE 1 ORAL
7583762 1016905423 C DICLOFENAC SODIUM 1 ORAL
7583762 1016905420 SS BLINDED TOCILIZUMAB 2 INTRAVENOUS PREVIOUSLY ENROLLED IN WA18063
7583762 1016905424 C DICLOFENAC SODIUM 1 ORAL
7583762 1016905425 C OMEPRAZOLE 1
7583762 1016905427 C ARTERIOSAN PLUS 2 1 TABLET
7583762 1016905426 C ATORVASTATIN 1
7583762 1016905428 C METHOTREXATE 1 ORAL FREQUENCY: AS MUCH AS NEEDED (QS)

Indications of drugs used

Event ID DRUG SEQ INDI PT
7583762 1016905419 RHEUMATOID ARTHRITIS
7583762 1016905420 RHEUMATOID ARTHRITIS

Outcome of event

Event ID OUTC COD
7583762 HO

Reactions reported

Event ID PT
7583762 CHEST PAIN

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
7583762 1016905419 20061221
7583762 1016905422 20100525
7583762 1016905421 20080212 20100522
7583762 1016905423 20080214 20100522
7583762 1016905424 20100525
7583762 1016905425 20080314 20080522
7583762 1016905427 20080212
7583762 1016905426 20080806