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
114039163 11403916 3 F 20150709 20160721 20150821 20160722 EXP BR-ROCHE-1623494 ROCHE 83.31 YR F Y 70.00000 KG 20160722 CN 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
114039163 11403916 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) U 125276 SOLUTION FOR INFUSION
114039163 11403916 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) U 125276 SOLUTION FOR INFUSION
114039163 11403916 3 C ATENOLOL. ATENOLOL 1 Unknown ONE TABLET, TWICE A DAY 0 25 MG TABLET BID
114039163 11403916 4 C ENALAPRIL ENALAPRIL 1 Unknown DAILY 0 10 MBQ TABLET QD
114039163 11403916 5 C TECNOMET METHOTREXATE 1 Unknown 0 /wk
114039163 11403916 6 C SIMVASTATIN. SIMVASTATIN 1 Unknown 0 20 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114039163 11403916 1 Rheumatoid arthritis
114039163 11403916 3 Hypertension
114039163 11403916 4 Hypertension
114039163 11403916 5 Arthritis
114039163 11403916 6 Hypertension

Outcome of event

Event ID CASEID OUTC COD
114039163 11403916 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
114039163 11403916 Fall
114039163 11403916 Fracture
114039163 11403916 Pelvic fracture
114039163 11403916 Pubis fracture
114039163 11403916 Upper limb fracture

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
114039163 11403916 1 20111104 0
114039163 11403916 2 20160505 0