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
101755528 10175552 8 F 201204 20160720 20140516 20160725 EXP CA-ROCHE-1076475 ROCHE 68.71 YR F Y 71.60000 KG 20160725 OT CA CA

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
101755528 10175552 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) 125276 560 MG SOLUTION FOR INFUSION
101755528 10175552 2 C PAMIDRONATE PAMIDRONATE DISODIUM 1 0
101755528 10175552 3 C ELTROXIN LEVOTHYROXINE 1 0
101755528 10175552 4 C ARAVA LEFLUNOMIDE 1 0
101755528 10175552 5 C ATACAND CANDESARTAN CILEXETIL 1 0
101755528 10175552 6 C FLUCONAZOLE. FLUCONAZOLE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101755528 10175552 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
101755528 10175552 OT
101755528 10175552 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
101755528 10175552 Cough
101755528 10175552 Dry eye
101755528 10175552 Eye ulcer
101755528 10175552 Eyelid ptosis
101755528 10175552 Oropharyngeal pain
101755528 10175552 Pneumonia
101755528 10175552 Weight increased

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
101755528 10175552 1 20101005 0