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
127231661 12723166 1 I 20160907 20160908 20160908 EXP CA-ROCHE-1827234 ROCHE 0.00 F Y 0.00000 20160908 OT 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
127231661 12723166 1 PS ACTEMRA TOCILIZUMAB 1 Unknown U 125276
127231661 12723166 2 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous U 0
127231661 12723166 3 SS ENBREL ETANERCEPT 1 Subcutaneous U 0
127231661 12723166 4 SS ORENCIA ABATACEPT 1 Unknown U 0
127231661 12723166 5 C METHOTREXATE. METHOTREXATE 1 Unknown 0
127231661 12723166 6 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127231661 12723166 1 Product used for unknown indication
127231661 12723166 2 Product used for unknown indication
127231661 12723166 3 Product used for unknown indication
127231661 12723166 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127231661 12723166 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127231661 12723166 Arthralgia
127231661 12723166 Drug ineffective
127231661 12723166 Hypersensitivity
127231661 12723166 Joint range of motion decreased
127231661 12723166 Joint swelling
127231661 12723166 Musculoskeletal pain
127231661 12723166 Musculoskeletal stiffness
127231661 12723166 Peripheral swelling
127231661 12723166 Tendon disorder

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found