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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127269201 | 12726920 | 1 | I | 20160906 | 20160908 | 20160908 | EXP | CA-ROCHE-1826522 | ROCHE | 68.00 | YR | F | Y | 45.00000 | KG | 20160909 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127269201 | 12726920 | 1 | PS | RITUXAN | RITUXIMAB | 1 | Intravenous (not otherwise specified) | U | 103705 | 1000 | MG | SOLUTION FOR INFUSION | |||||||
| 127269201 | 12726920 | 2 | SS | ACTEMRA | TOCILIZUMAB | 1 | Intravenous (not otherwise specified) | U | 125276 | 375 | MG | SOLUTION FOR INFUSION | /month | ||||||
| 127269201 | 12726920 | 3 | SS | CELEBREX | CELECOXIB | 1 | Unknown | U | 0 | CAPSULE | |||||||||
| 127269201 | 12726920 | 4 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | U | 0 | ||||||||||
| 127269201 | 12726920 | 5 | C | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Oral | 0 | 650 | MG | |||||||||
| 127269201 | 12726920 | 6 | C | DIPHENHYDRAMINE HYDROCHLORIDE. | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Oral | 0 | 50 | MG | |||||||||
| 127269201 | 12726920 | 7 | C | FOLIC ACID. | FOLIC ACID | 1 | Unknown | 0 | |||||||||||
| 127269201 | 12726920 | 8 | C | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | Intravenous (not otherwise specified) | 0 | 100 | MG | |||||||||
| 127269201 | 12726920 | 9 | C | VENLAFAXINE HYDROCHLORIDE. | VENLAFAXINE HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127269201 | 12726920 | 1 | Rheumatoid arthritis |
| 127269201 | 12726920 | 2 | Rheumatoid arthritis |
| 127269201 | 12726920 | 3 | Product used for unknown indication |
| 127269201 | 12726920 | 4 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127269201 | 12726920 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127269201 | 12726920 | Abdominal pain | |
| 127269201 | 12726920 | Amnesia | |
| 127269201 | 12726920 | Arthralgia | |
| 127269201 | 12726920 | Cough | |
| 127269201 | 12726920 | Fatigue | |
| 127269201 | 12726920 | Fungal infection | |
| 127269201 | 12726920 | Headache | |
| 127269201 | 12726920 | Nausea | |
| 127269201 | 12726920 | Pain in extremity | |
| 127269201 | 12726920 | Photosensitivity reaction | |
| 127269201 | 12726920 | Stress | |
| 127269201 | 12726920 | Tendonitis | |
| 127269201 | 12726920 | Urinary tract infection | |
| 127269201 | 12726920 | Weight decreased | |
| 127269201 | 12726920 | White blood cell count decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |