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
125644253 12564425 3 F 20160802 20160718 20160810 EXP CA-AMGEN-CANSP2016091040 AMGEN 55.00 YR A F Y 0.00000 20160810 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
125644253 12564425 1 PS ENBREL ETANERCEPT 1 Unknown UNK U 103795 UNKNOWN FORMULATION
125644253 12564425 2 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown UNK 0
125644253 12564425 3 SS REMICADE INFLIXIMAB 1 Unknown UNK 0
125644253 12564425 4 SS RITUXAN RITUXIMAB 1 Unknown UNK 0
125644253 12564425 5 SS TYLENOL WITH CODEINE ACETAMINOPHENCODEINE PHOSPHATE 1 Unknown UNK 0 TABLET
125644253 12564425 6 C ACTEMRA TOCILIZUMAB 1 Unknown UNK 0
125644253 12564425 7 C ARAVA LEFLUNOMIDE 1 Unknown UNK 0 TABLET
125644253 12564425 8 C HUMIRA ADALIMUMAB 1 Unknown 0
125644253 12564425 9 C ARTHROTEC DICLOFENAC SODIUMMISOPROSTOL 1 Unknown UNK 0 TABLET
125644253 12564425 10 C LYRICA PREGABALIN 1 Unknown UNK 0 CAPSULE
125644253 12564425 11 C METHOTREXATE. METHOTREXATE 1 Unknown UNK 0
125644253 12564425 12 C ORENCIA ABATACEPT 1 Unknown UNK 0
125644253 12564425 13 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0 TABLET
125644253 12564425 14 C RABEPRAZOLE RABEPRAZOLE 1 Unknown UNK 0
125644253 12564425 15 C SIMPONI GOLIMUMAB 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125644253 12564425 1 Rheumatoid arthritis
125644253 12564425 2 Rheumatoid arthritis
125644253 12564425 3 Rheumatoid arthritis
125644253 12564425 4 Rheumatoid arthritis
125644253 12564425 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125644253 12564425 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125644253 12564425 Activities of daily living impaired
125644253 12564425 Blood cholesterol increased
125644253 12564425 Drug ineffective
125644253 12564425 Hypersensitivity
125644253 12564425 Insomnia
125644253 12564425 Pain
125644253 12564425 Rheumatoid arthritis
125644253 12564425 Swelling

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

no results found

Therapies reported

no results found