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
124549732 12454973 2 F 201502 20160706 20160610 20160707 EXP DE-ROCHE-1773133 ROCHE 46.43 YR F Y 0.00000 20160707 MD DE DE

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
124549732 12454973 1 PS MABTHERA RITUXIMAB 1 Unknown N 103705 500 MG
124549732 12454973 2 SS MABTHERA RITUXIMAB 1 Unknown N 103705
124549732 12454973 3 C PREDNISOLON PREDNISOLONE 1 Oral 0 100 MG
124549732 12454973 4 C PREDNISOLON PREDNISOLONE 1 Unknown 0 5 MG
124549732 12454973 5 C METHOTREXATE. METHOTREXATE 1 Oral 0 2.5 MG
124549732 12454973 6 C VALSARTAN. VALSARTAN 1 Oral 0 80 MG
124549732 12454973 7 C METAMIZOL METAMIZOLE SODIUM 1 Oral 0 1500 MG
124549732 12454973 8 C VITAMIN D3 CHOLECALCIFEROL 1 Oral 0 2000 IU /wk
124549732 12454973 9 C COTRIMOXAZOLE SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 0 960 MG TIW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124549732 12454973 1 Rheumatoid arthritis
124549732 12454973 6 Hypertension
124549732 12454973 8 Osteoporosis prophylaxis
124549732 12454973 9 Infection prophylaxis

Outcome of event

Event ID CASEID OUTC COD
124549732 12454973 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124549732 12454973 Pulmonary fibrosis

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
124549732 12454973 1 20150117 20150117 0
124549732 12454973 2 20150131 20150131 0
124549732 12454973 3 20141125 0
124549732 12454973 5 201508 0
124549732 12454973 9 20141125 0