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
116921265 11692126 5 F 2011 20160728 20151103 20160805 EXP CA-AMGEN-CANSP2015114671 AMGEN 51.00 YR A F Y 63.00000 KG 20160805 MD 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
116921265 11692126 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, QWK U 103795 50 MG UNKNOWN FORMULATION /wk
116921265 11692126 2 SS PREDNISONE. PREDNISONE 1 Unknown UNK 0
116921265 11692126 3 SS METHOTREXATE. METHOTREXATE 1 Subcutaneous 25 MG, UNK 0 25 MG
116921265 11692126 4 SS METHOTREXATE. METHOTREXATE 1 Oral 2.5 MG, 8 TABLETS ONCE A WEEK X 2 0 2.5 MG
116921265 11692126 5 SS METHOTREXATE. METHOTREXATE 1 Oral 15 MG, QWK 0 15 MG /wk
116921265 11692126 6 SS METHOTREXATE. METHOTREXATE 1 Subcutaneous 20 MG, QWK 0 20 MG /wk
116921265 11692126 7 C VIMOVO ESOMEPRAZOLE MAGNESIUMNAPROXEN 1 500-20 MG TABLET 1 TABLET(S) TWO TIMES DAILY 0 TABLET BID
116921265 11692126 8 C FOLIC ACID. FOLIC ACID 1 5 MG, QWK 0 5 MG /wk
116921265 11692126 9 C NAPROXEN. NAPROXEN 1 Oral 500 MG, BID 0 500 MG BID
116921265 11692126 10 C HUMIRA ADALIMUMAB 1 Unknown UNK 0
116921265 11692126 11 C HUMIRA ADALIMUMAB 1 Subcutaneous 40 MG, QWK 0 40 MG /wk
116921265 11692126 12 C ACTEMRA TOCILIZUMAB 1 UNK 0
116921265 11692126 13 C DEPO-MEDROL METHYLPREDNISOLONE ACETATE 1 Intra-articular 80 MG, UNK 0 80 MG INJECTION
116921265 11692126 14 C LYRICA PREGABALIN 1 Oral 150 MG, BID 0 150 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116921265 11692126 1 Rheumatoid arthritis
116921265 11692126 2 Rheumatoid arthritis
116921265 11692126 3 Rheumatoid arthritis
116921265 11692126 9 Arthralgia
116921265 11692126 13 Rheumatoid arthritis
116921265 11692126 14 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
116921265 11692126 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116921265 11692126 Abdominal pain
116921265 11692126 Activities of daily living impaired
116921265 11692126 Arthralgia
116921265 11692126 Chest pain
116921265 11692126 Condition aggravated
116921265 11692126 Drug ineffective
116921265 11692126 Dry eye
116921265 11692126 Dyspnoea
116921265 11692126 Eye irritation
116921265 11692126 Eye pain
116921265 11692126 Fatigue
116921265 11692126 Fibromyalgia
116921265 11692126 Gait disturbance
116921265 11692126 Infection
116921265 11692126 Interstitial lung disease
116921265 11692126 Joint crepitation
116921265 11692126 Joint swelling
116921265 11692126 Lung disorder
116921265 11692126 Mass
116921265 11692126 Maternal exposure during pregnancy
116921265 11692126 Mobility decreased
116921265 11692126 Musculoskeletal pain
116921265 11692126 Musculoskeletal stiffness
116921265 11692126 Nausea
116921265 11692126 Nervousness
116921265 11692126 Nodule
116921265 11692126 Ocular hyperaemia
116921265 11692126 Osteoarthritis
116921265 11692126 Pain
116921265 11692126 Pain in extremity
116921265 11692126 Photophobia
116921265 11692126 Pleuritic pain
116921265 11692126 Rheumatoid arthritis
116921265 11692126 Swelling
116921265 11692126 Synovial cyst
116921265 11692126 Tenosynovitis stenosans

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
116921265 11692126 1 200812 201007 0
116921265 11692126 3 2008 0
116921265 11692126 4 201409 0
116921265 11692126 6 2014 0
116921265 11692126 7 20140911 0
116921265 11692126 8 20140911 0
116921265 11692126 11 201008 201312 0
116921265 11692126 12 2014 0