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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123299002 | 12329900 | 2 | F | 20160817 | 20160503 | 20160825 | EXP | CA-AMGEN-CANSP2016055569 | AMGEN | 0.00 | F | Y | 0.00000 | 20160825 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123299002 | 12329900 | 1 | PS | ENBREL | ETANERCEPT | 1 | Subcutaneous | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
123299002 | 12329900 | 2 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | UNK | 0 | TABLET | |||||||||
123299002 | 12329900 | 3 | SS | ASPIRIN. | ASPIRIN | 1 | Unknown | UNK | 0 | ||||||||||
123299002 | 12329900 | 4 | SS | DICLOFENAC | DICLOFENAC | 1 | Unknown | UNK | 0 | ||||||||||
123299002 | 12329900 | 5 | SS | GOLD | GOLD | 1 | Unknown | UNK | 0 | ||||||||||
123299002 | 12329900 | 6 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNK | 0 | ||||||||||
123299002 | 12329900 | 7 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | UNK | 0 | ||||||||||
123299002 | 12329900 | 8 | SS | MOTRIN | IBUPROFEN | 1 | Unknown | UNK | 0 | ||||||||||
123299002 | 12329900 | 9 | SS | NAPROSYN | NAPROXEN | 1 | Unknown | UNK | 0 | ||||||||||
123299002 | 12329900 | 10 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | UNK | 0 | TABLET | |||||||||
123299002 | 12329900 | 11 | C | TRAMADOL. | TRAMADOL | 1 | Unknown | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
123299002 | 12329900 | 1 | Rheumatoid arthritis |
123299002 | 12329900 | 2 | Rheumatoid arthritis |
123299002 | 12329900 | 3 | Rheumatoid arthritis |
123299002 | 12329900 | 4 | Rheumatoid arthritis |
123299002 | 12329900 | 5 | Rheumatoid arthritis |
123299002 | 12329900 | 6 | Rheumatoid arthritis |
123299002 | 12329900 | 7 | Rheumatoid arthritis |
123299002 | 12329900 | 8 | Rheumatoid arthritis |
123299002 | 12329900 | 9 | Rheumatoid arthritis |
123299002 | 12329900 | 10 | Rheumatoid arthritis |
123299002 | 12329900 | 11 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
123299002 | 12329900 | OT |
123299002 | 12329900 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
123299002 | 12329900 | Adverse reaction | |
123299002 | 12329900 | Deafness transitory | |
123299002 | 12329900 | Decreased appetite | |
123299002 | 12329900 | Dizziness | |
123299002 | 12329900 | Ear infection | |
123299002 | 12329900 | Foot operation | |
123299002 | 12329900 | Gastrointestinal pain | |
123299002 | 12329900 | Headache | |
123299002 | 12329900 | Hypophagia | |
123299002 | 12329900 | Nausea | |
123299002 | 12329900 | Pharyngitis | |
123299002 | 12329900 | Shoulder arthroplasty | |
123299002 | 12329900 | Vomiting | |
123299002 | 12329900 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |