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
125315241 12531524 1 I 20160621 20160706 20160706 EXP CA-HQ SPECIALTY-CA-2016INT000468 INTERCHEM 53.00 YR F Y 0.00000 20160706 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
125315241 12531524 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Oral UNK Y 201749
125315241 12531524 2 SS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Subcutaneous UNK Y 201749
125315241 12531524 3 SS ACTEMRA TOCILIZUMAB 1 UNK Y 0
125315241 12531524 4 SS CIMZIA CERTOLIZUMAB PEGOL 1 UNK Y 0
125315241 12531524 5 SS PLAQUENIL /00072602/ HYDROXYCHLOROQUINE DIPHOSPHATE 1 UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125315241 12531524 1 Rheumatoid arthritis
125315241 12531524 3 Rheumatoid arthritis
125315241 12531524 4 Product used for unknown indication
125315241 12531524 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125315241 12531524 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125315241 12531524 Chest X-ray abnormal
125315241 12531524 Dental caries
125315241 12531524 Drug ineffective
125315241 12531524 Lower respiratory tract infection
125315241 12531524 Malaise
125315241 12531524 Nausea

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
125315241 12531524 3 201508 0