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
126739901 12673990 1 I 20160817 20160822 20160822 EXP CA-AMGEN-CANSP2016107934 AMGEN 0.00 F Y 0.00000 20160822 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
126739901 12673990 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
126739901 12673990 2 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown UNK 0
126739901 12673990 3 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK 0
126739901 12673990 4 SS ORENCIA ABATACEPT 1 Unknown UNK 0
126739901 12673990 5 C METHOTREXATE. METHOTREXATE 1 UNK 0
126739901 12673990 6 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 UNK 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126739901 12673990 1 Product used for unknown indication
126739901 12673990 2 Product used for unknown indication
126739901 12673990 3 Product used for unknown indication
126739901 12673990 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126739901 12673990 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126739901 12673990 Arthralgia
126739901 12673990 Drug ineffective
126739901 12673990 Hypersensitivity
126739901 12673990 Joint range of motion decreased
126739901 12673990 Joint swelling
126739901 12673990 Musculoskeletal pain
126739901 12673990 Musculoskeletal stiffness
126739901 12673990 Peripheral swelling
126739901 12673990 Tendon disorder

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

no results found

Therapies reported

no results found