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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126261781 | 12626178 | 1 | I | 20160721 | 20160805 | 20160805 | EXP | E2B_00531494 | CA-HQ SPECIALTY-CA-2016INT000691 | INTERCHEM | 53.00 | YR | F | Y | 0.00000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126261781 | 12626178 | 1 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | UNK | U | 201749 | |||||||||
| 126261781 | 12626178 | 2 | SS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 0 | |||||||||
| 126261781 | 12626178 | 3 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | UNK | U | 0 | |||||||||
| 126261781 | 12626178 | 4 | SS | CIMZIA | CERTOLIZUMAB PEGOL | 1 | Unknown | UNK | U | 0 | |||||||||
| 126261781 | 12626178 | 5 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNK | U | 0 | |||||||||
| 126261781 | 12626178 | 6 | SS | PLAQUENIL /00072602/ | HYDROXYCHLOROQUINE DIPHOSPHATE | 1 | Unknown | UNK | U | 0 | |||||||||
| 126261781 | 12626178 | 7 | SS | PROCYTOX | CYCLOPHOSPHAMIDE | 1 | Unknown | UNK | U | 0 | |||||||||
| 126261781 | 12626178 | 8 | SS | REMICADE | INFLIXIMAB | 1 | Unknown | UNK | U | 0 | |||||||||
| 126261781 | 12626178 | 9 | SS | SIMPONI | GOLIMUMAB | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126261781 | 12626178 | 1 | Product used for unknown indication |
| 126261781 | 12626178 | 2 | Product used for unknown indication |
| 126261781 | 12626178 | 3 | Product used for unknown indication |
| 126261781 | 12626178 | 4 | Product used for unknown indication |
| 126261781 | 12626178 | 5 | Product used for unknown indication |
| 126261781 | 12626178 | 6 | Product used for unknown indication |
| 126261781 | 12626178 | 7 | Product used for unknown indication |
| 126261781 | 12626178 | 8 | Product used for unknown indication |
| 126261781 | 12626178 | 9 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126261781 | 12626178 | OT |
| 126261781 | 12626178 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126261781 | 12626178 | Bone erosion | |
| 126261781 | 12626178 | Bronchiectasis | |
| 126261781 | 12626178 | Disease susceptibility | |
| 126261781 | 12626178 | Drug ineffective | |
| 126261781 | 12626178 | Joint swelling | |
| 126261781 | 12626178 | Myocardial infarction | |
| 126261781 | 12626178 | Pulmonary fibrosis | |
| 126261781 | 12626178 | Toxicity to various agents | |
| 126261781 | 12626178 | Upper limb fracture |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |