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
122096537 12209653 7 F 2013 20160923 20160325 20160927 EXP CA-ROCHE-1213265 ROCHE 76.36 YR F Y 65.00000 KG 20160927 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
122096537 12209653 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) B20152,B20112,B20172,B2027B19,B2032 125276 520 MG SOLUTION FOR INFUSION
122096537 12209653 2 C APO-FOLIC 2 0
122096537 12209653 3 C APO-GLYBURIDE GLYBURIDE 1 0
122096537 12209653 4 C CELEBREX CELECOXIB 1 0
122096537 12209653 5 C METFORMIN METFORMIN HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122096537 12209653 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
122096537 12209653 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122096537 12209653 Arthralgia
122096537 12209653 Blood pressure fluctuation
122096537 12209653 Blood pressure increased
122096537 12209653 Blood pressure systolic increased
122096537 12209653 Body temperature increased
122096537 12209653 Eye disorder
122096537 12209653 Hypertension
122096537 12209653 Influenza
122096537 12209653 Infusion related reaction
122096537 12209653 Joint swelling
122096537 12209653 Nasopharyngitis
122096537 12209653 Pain
122096537 12209653 Pruritus
122096537 12209653 Tibia 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
122096537 12209653 1 20121113 0