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
125375902 12537590 2 F 201604 20160720 20160707 20160803 EXP CA-HQ SPECIALTY-CA-2016INT000471 INTERCHEM 54.00 YR F Y 0.00000 20160803 CN 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
125375902 12537590 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral 2.8571 MG (20 MG,1 IN 1 W) 201749
125375902 12537590 2 SS ENBREL ETANERCEPT 1 Subcutaneous UNK 0
125375902 12537590 3 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0
125375902 12537590 4 SS HUMIRA ADALIMUMAB 1 Unknown UNK Y 0
125375902 12537590 5 SS ORENCIA ABATACEPT 1 Unknown UNK Y 0
125375902 12537590 6 SS XELJANZ TOFACITINIB CITRATE 1 Oral 10 MG (5 MG, 2 IN 1 D) 0 5 MG
125375902 12537590 7 C HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 UNK U 0
125375902 12537590 8 C TETANUS TOXOID ADSORBED CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED) 1 UNK U 0
125375902 12537590 9 C HAEMOPHILUS INFLUENZA TYPE B VACCINE HAEMOPHILUS INFLUENZAE TYPE B 1 UNK U 0
125375902 12537590 10 C PREVNAR PNEUMOCOCCAL 7-VALENT CONJUGATE VACCINE (DIPHTHERIA CRM197 PROTEIN) 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125375902 12537590 1 Rheumatoid arthritis
125375902 12537590 2 Rheumatoid arthritis
125375902 12537590 3 Rheumatoid arthritis
125375902 12537590 4 Rheumatoid arthritis
125375902 12537590 5 Product used for unknown indication
125375902 12537590 6 Rheumatoid arthritis
125375902 12537590 7 Product used for unknown indication
125375902 12537590 8 Product used for unknown indication
125375902 12537590 9 Product used for unknown indication
125375902 12537590 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125375902 12537590 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125375902 12537590 Drug ineffective
125375902 12537590 Epicondylitis
125375902 12537590 Malaise
125375902 12537590 Rheumatoid arthritis

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
125375902 12537590 2 201406 0
125375902 12537590 4 20050101 20080101 0
125375902 12537590 5 2010 2014 0
125375902 12537590 6 20160627 0
125375902 12537590 8 20160524 0
125375902 12537590 9 20160524 0
125375902 12537590 10 20160524 0