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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122616093 | 12261609 | 3 | F | 20130527 | 20160630 | 20160412 | 20160705 | EXP | CA-ROCHE-1230738 | ROCHE | 59.03 | YR | F | Y | 65.90000 | KG | 20160705 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122616093 | 12261609 | 1 | PS | RITUXAN | RITUXIMAB | 1 | Intravenous (not otherwise specified) | N | B62482,H0760 | 103705 | 1000 | MG | SOLUTION FOR INFUSION | ||||||
| 122616093 | 12261609 | 2 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | U | 0 | ||||||||||
| 122616093 | 12261609 | 3 | C | TYLENOL WITH CODEINE | ACETAMINOPHENCODEINE PHOSPHATE | 1 | 0 | ||||||||||||
| 122616093 | 12261609 | 4 | C | DIPHENHYDRAMINE HCL | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | Oral | 0 | 50 | MG | |||||||||
| 122616093 | 12261609 | 5 | C | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | Intravenous (not otherwise specified) | 0 | 100 | MG | |||||||||
| 122616093 | 12261609 | 6 | C | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | Oral | 0 | 650 | MG | |||||||||
| 122616093 | 12261609 | 7 | C | COVERSYL | PERINDOPRIL | 1 | Unknown | 0 | 4 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122616093 | 12261609 | 1 | Rheumatoid arthritis |
| 122616093 | 12261609 | 2 | Product used for unknown indication |
| 122616093 | 12261609 | 4 | Premedication |
| 122616093 | 12261609 | 5 | Premedication |
| 122616093 | 12261609 | 6 | Premedication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122616093 | 12261609 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122616093 | 12261609 | Blood pressure fluctuation | |
| 122616093 | 12261609 | Blood pressure increased | |
| 122616093 | 12261609 | Heart rate decreased | |
| 122616093 | 12261609 | Heart rate increased | |
| 122616093 | 12261609 | Infusion related reaction | |
| 122616093 | 12261609 | Interstitial lung disease | |
| 122616093 | 12261609 | Osteoporosis | |
| 122616093 | 12261609 | Oxygen saturation decreased | |
| 122616093 | 12261609 | Pneumothorax | |
| 122616093 | 12261609 | Throat irritation | |
| 122616093 | 12261609 | Weight 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 |
|---|---|---|---|---|---|---|
| 122616093 | 12261609 | 1 | 20130527 | 0 | ||
| 122616093 | 12261609 | 4 | 20130527 | 0 | ||
| 122616093 | 12261609 | 5 | 20130527 | 0 | ||
| 122616093 | 12261609 | 6 | 20130527 | 0 |