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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124878693 | 12487869 | 3 | F | 2015 | 20160719 | 20160622 | 20160727 | EXP | CA-PFIZER INC-2015277299 | PFIZER | 71.00 | YR | F | Y | 0.00000 | 20160727 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124878693 | 12487869 | 1 | PS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 2X/DAY | Y | 203214 | 5 | MG | TABLET | BID | |||||
| 124878693 | 12487869 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | UNK | 11719 | SOLUTION FOR INJECTION | ||||||||||
| 124878693 | 12487869 | 3 | SS | ALENDRONATE | ALENDRONATE SODIUM | 1 | UNK | 0 | |||||||||||
| 124878693 | 12487869 | 4 | SS | PREDNISONE. | PREDNISONE | 1 | UNK | 0 | |||||||||||
| 124878693 | 12487869 | 5 | C | VOLTAREN | DICLOFENAC SODIUM | 1 | UNK | 0 | |||||||||||
| 124878693 | 12487869 | 6 | C | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | Oral | 200 MG, 2X/DAY | 0 | 200 | MG | BID | |||||||
| 124878693 | 12487869 | 7 | C | TYLENOL | ACETAMINOPHEN | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124878693 | 12487869 | 1 | Rheumatoid arthritis |
| 124878693 | 12487869 | 2 | Rheumatoid arthritis |
| 124878693 | 12487869 | 3 | Osteoporosis |
| 124878693 | 12487869 | 5 | Musculoskeletal pain |
| 124878693 | 12487869 | 7 | Osteoarthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124878693 | 12487869 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124878693 | 12487869 | Abdominal discomfort | |
| 124878693 | 12487869 | Arthralgia | |
| 124878693 | 12487869 | Arthritis infective | |
| 124878693 | 12487869 | Limb discomfort | |
| 124878693 | 12487869 | Musculoskeletal discomfort | |
| 124878693 | 12487869 | Musculoskeletal pain | |
| 124878693 | 12487869 | Musculoskeletal stiffness | |
| 124878693 | 12487869 | Myalgia | |
| 124878693 | 12487869 | Neck pain | |
| 124878693 | 12487869 | Pain in extremity | |
| 124878693 | 12487869 | Paraesthesia | |
| 124878693 | 12487869 | Peripheral swelling | |
| 124878693 | 12487869 | Pruritus | |
| 124878693 | 12487869 | Rash macular | |
| 124878693 | 12487869 | Spinal pain | |
| 124878693 | 12487869 | Toothache | |
| 124878693 | 12487869 | Urinary incontinence | |
| 124878693 | 12487869 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 124878693 | 12487869 | 1 | 20150720 | 20160608 | 0 |