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
127074891 12707489 1 I 2016 20160823 20160901 20160901 EXP US-AMGEN-USASL2016112357 AMGEN 53.00 YR A F Y 0.00000 20160901 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
127074891 12707489 1 PS ENBREL ETANERCEPT 1 Unknown UNK Y 1064418 103795 UNKNOWN FORMULATION
127074891 12707489 2 SS METHOTREXATE. METHOTREXATE 1 Unknown UNK 0
127074891 12707489 3 SS CELEBREX CELECOXIB 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127074891 12707489 1 Rheumatoid arthritis
127074891 12707489 2 Product used for unknown indication
127074891 12707489 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127074891 12707489 HO
127074891 12707489 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127074891 12707489 Diverticulitis
127074891 12707489 Diverticulum
127074891 12707489 Drug effect incomplete
127074891 12707489 Injection site erythema
127074891 12707489 Musculoskeletal stiffness
127074891 12707489 Myalgia
127074891 12707489 Osteoarthritis

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

no results found

Therapies reported

no results found