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
99182488 9918248 8 F 20141001 20160831 20140224 20160902 EXP CA-ROCHE-1354333 ROCHE 56.33 YR F Y 83.40000 KG 20160902 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
99182488 9918248 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 640 MG SOLUTION FOR INFUSION
99182488 9918248 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 SOLUTION FOR INFUSION
99182488 9918248 3 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 SOLUTION FOR INFUSION
99182488 9918248 4 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) Y 125276 320 MG SOLUTION FOR INFUSION
99182488 9918248 5 C PREDNISONE. PREDNISONE 1 0
99182488 9918248 6 C ACETYLSALICYLIC ACID ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
99182488 9918248 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
99182488 9918248 OT
99182488 9918248 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
99182488 9918248 Bronchitis
99182488 9918248 Nasopharyngitis
99182488 9918248 Pain
99182488 9918248 Sinusitis
99182488 9918248 Tooth abscess
99182488 9918248 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
99182488 9918248 1 20130717 0
99182488 9918248 2 20150211 0
99182488 9918248 3 20160606 0
99182488 9918248 4 20140422 0