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
105920528 10592052 8 F 201410 20160725 20141119 20160726 EXP BR-ROCHE-1475268 ROCHE 53.82 YR M Y 90.00000 KG 20160727 MD BR BR

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
105920528 10592052 1 PS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) RECENT DOSE ON 22MAY2014 (DAY 15) U 103705 SOLUTION FOR INFUSION
105920528 10592052 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) 125276 SOLUTION FOR INFUSION
105920528 10592052 3 SS CIPROFLOXACIN HYDROCHLORIDE. CIPROFLOXACIN HYDROCHLORIDE 1 Unknown 0
105920528 10592052 4 C PREDNISONE. PREDNISONE 1 Unknown 0 20 MG
105920528 10592052 5 C PREDNISONE. PREDNISONE 1 Unknown 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105920528 10592052 1 Rheumatoid arthritis
105920528 10592052 2 Rheumatoid arthritis
105920528 10592052 3 Furuncle
105920528 10592052 4 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
105920528 10592052 HO
105920528 10592052 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
105920528 10592052 Adenoidal hypertrophy
105920528 10592052 Arthralgia
105920528 10592052 Bronchospasm
105920528 10592052 Cholelithiasis
105920528 10592052 Drug ineffective
105920528 10592052 Dyspnoea
105920528 10592052 Erythema
105920528 10592052 Furuncle
105920528 10592052 Joint swelling
105920528 10592052 Neck pain
105920528 10592052 Peripheral swelling
105920528 10592052 Pneumonia
105920528 10592052 Spinal pain
105920528 10592052 Therapeutic response decreased

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
105920528 10592052 1 20131210 20141001 0
105920528 10592052 2 20151101 0