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
110366244 11036624 4 F 201303 20160811 20150416 20160818 EXP US-AMGEN-USASP2015035638 AMGEN 74.00 YR E F Y 0.00000 20160818 MD US US

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
110366244 11036624 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK 1034025 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
110366244 11036624 2 SS ENBREL ETANERCEPT 1 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
110366244 11036624 3 SS ORENCIA ABATACEPT 1 Unknown UNK 0
110366244 11036624 4 SS METHOTREXATE. METHOTREXATE 1 Unknown 2.4 MG, QWK 0 2.4 MG TABLET /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110366244 11036624 1 Rheumatoid arthritis
110366244 11036624 2 Psoriasis
110366244 11036624 3 Product used for unknown indication
110366244 11036624 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
110366244 11036624 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110366244 11036624 Arthralgia
110366244 11036624 Contusion
110366244 11036624 Fall
110366244 11036624 Fatigue
110366244 11036624 Hepatic enzyme increased
110366244 11036624 Impaired healing
110366244 11036624 Joint injury
110366244 11036624 Laboratory test abnormal
110366244 11036624 Mobility decreased
110366244 11036624 Nausea
110366244 11036624 Osteoarthritis
110366244 11036624 Peripheral swelling
110366244 11036624 Precancerous skin lesion
110366244 11036624 Skin cancer

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

no results found

Therapies reported

no results found