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
126246971 12624697 1 I 20160715 20160805 20160805 PER US-PFIZER INC-2016349829 PFIZER 45.00 YR F Y 0.00000 20160805 CN US US

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
126246971 12624697 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK 11719
126246971 12624697 2 SS IMURAN AZATHIOPRINE 1 50 MG, UNK 0 50 MG
126246971 12624697 3 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) 1000 MG, UNK 0 1000 MG
126246971 12624697 4 SS ACTEMRA TOCILIZUMAB 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126246971 12624697 1 Rheumatoid arthritis
126246971 12624697 2 Rheumatoid arthritis
126246971 12624697 3 Rheumatoid arthritis
126246971 12624697 4 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126246971 12624697 Drug ineffective

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
126246971 12624697 1 201502 201508 0
126246971 12624697 2 201508 201604 0
126246971 12624697 3 201412 201505 0
126246971 12624697 4 201505 201508 0