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
105531773 10553177 3 F 20160818 20141030 20160819 EXP CA-ROCHE-1359497 ROCHE 0.00 F Y 0.00000 20160819 MD 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
105531773 10553177 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) 125276 480 MG SOLUTION FOR INFUSION
105531773 10553177 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) 125276 534 MG SOLUTION FOR INFUSION
105531773 10553177 3 C CELEBREX CELECOXIB 1 0
105531773 10553177 4 C PROZAC FLUOXETINE HYDROCHLORIDE 1 0
105531773 10553177 5 C METHOTREXATE. METHOTREXATE 1 0
105531773 10553177 6 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 0
105531773 10553177 7 C FOLIC ACID. FOLIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105531773 10553177 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
105531773 10553177 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
105531773 10553177 Contusion
105531773 10553177 Joint swelling
105531773 10553177 Nasopharyngitis

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
105531773 10553177 1 20140116 20140904 0
105531773 10553177 2 20160726 0