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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
82116752 | 8211675 | 2 | F | 2010 | 20121115 | 20111029 | 20130930 | PER | US-AMGEN-USASP2011010479 | AMGEN | 58.00 | YR | F | Y | 0.00000 | 20130930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
82116752 | 8211675 | 1 | PS | Enbrel | 1 | 50 MG, QWK | D | 103795 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk | |||||||
82116752 | 8211675 | 2 | C | METHOTREXATE | 1 | UNK MG, QWK | D | 0 | /wk | ||||||||||
82116752 | 8211675 | 3 | C | PREDNISONE /00044702/ | 1 | UNK MG, UNK | D | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
82116752 | 8211675 | 1 | Rheumatoid arthritis |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
82116752 | 8211675 | Arthralgia | |
82116752 | 8211675 | Bunion | |
82116752 | 8211675 | Therapeutic response decreased |
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 |
---|---|---|---|---|---|---|
82116752 | 8211675 | 1 | 20000201 | 201209 | 0 |